Sterilizing-grade Durapore®0.1 μm and 0.22 μm Hydrophilic Filters Superior filters for the sterile filtrationof biopharmaceutical liquids

Data Sheet

A trusted name in the industry for over 30 years, Durapore® sterilizing-grade 0.1 μm and 0.22 μm hydrophilic polyvinylidene fluoride (PVDF) membranes are low protein binding and provide sterility assurance, high flow rates and throughputs.

The Durapore® membrane contributes to clean processes due to low extracta-bles, broad chemical compatibility, and its non-fiber releasing properties.

Benefits• Low protein binding membrane yields high protein

recovery with minimal loss of valuable product

• Superior membrane for filtration processes requiring high flow rates and throughputs

• Ideal for designing scalable solutions from bench top to full-scale manufacturing

Membrane TypesDurapore® hydrophilic membrane• 0.1 μm hydrophilic

• 0.22 μm hydrophilic

Filter Formats• OptiScale® small-scale disposable capsule filters

• Millipak® low-volume capsule filters

• Opticap® XL and XLT disposable capsule filters

• Cartridge filters

EMD Millipore Corp. is a subsidiary of Merck KGaA, Darmstadt, Germany

Regulatory ComplianceFilters with hydrophilic Durapore® membranes are designed, developed, and manufactured in accordance with a Quality Management System approved by an accredited registering body to an ISO® 9001 Quality Systems Standard. Each Durapore® filter is shipped with a Certificate of Quality. Each cartridge filter and Millipak®, Opticap® XL and Opticap® XLT capsule filter is integrity tested during manufacturing and is sup-ported with a Validation Guide for compliance with regulatory requirements. For traceability and easy identification, each device is marked with the product name and identifying characteristics.

Multiple Formats AvailableSterilizing-grade hydrophilic Durapore® membranes are available in four formats, two pore sizes, and multiple configurations that vary by filtration area and type of inlet/outlet connection. We have a format to meet your application needs.

OptiScale® Process Development Screening ToolOptiScale® disposable capsule filters provide a convenient small volume option for process screening and scaling. These “drop in” filters are ideal for evaluating biophar-maceuticals. OptiScale® capsule filters offer speed-to-market strategies for efficiently developing compounds and biotherapeutics.

The OptiScale® disposable capsule is ideally suited for process development and screening. OptiScale® capsules are faster and easier to set up than conventional 25 mm and 47 mm discs.

Millipak® Low-Volume Capsule FiltersMillipak® filters with hydrophilic Durapore® membranes are uniquely designed for the removal of particles and microorganisms. The stacked disc design allows minimal hold-up volume and no particle shedding, making Millipak® units ideally suited for high value-added applications such as sterile finish and fill. Each Millipak® filter is integrity tested during the manufacturing process.

Millipak® filters are available in two different stack sizes. Adjustable, easy-to-turn, up-stream vents and drain valves with hose barb connections allow for easy process control.

Cartridge FiltersHydrophilic Durapore® cartridge filters provide high throughput with minimal differ-ential pressure. Cartridges are robust, strong, resilient and are designed to withstand multiple steam-in-place cycles. Each Durapore® cartridge filter is integrity tested dur-ing the manufacturing process.

A full range of filtration areas is available to suit varying application requirements and a variety of connection options are offered to meet your application and housing requirements.

OptiScale® Filters

Cartridge Filters

Millipak® Filters

Opticap® XL and XLT Disposable Capsule FiltersConvenient and Easy to Use Opticap® XL and XLT capsule filters eliminate the time and expense associated with assembling, cleaning, and validating stainless steel housings. Adjustable, easy-to-turn, upstream vents and drain valve with O-ring seals and hose barb connections allow for easy process control. Other ease-of-use features include flow direction arrows and ribbed housing for easy gripping even with gloved hands.

The Right Size A wide range of filtration areas is available to fit all of your application needs and to allow easy scale-up of your small volume filtration steps to larger, full-scale filtration processes.

The Right Connections Self-contained and disposable, Opticap® XL and XLT capsule filters are supplied with a choice of inlet and outlet connections to optimize your filtration process, including sani-tary flanges which provide a high flow rate, fractional sanitary flanges and hose barbs.

Proven Integrity Each capsule is integrity tested during the manufacturing process to ensure reliable performance in your process.

Robust Construction Opticap® XL and XLT capsule design allows unparalleled thermal and hydraulic stress resistance in a disposable filter, resulting in reliability, high confidence in the steriliza-tion process, and improved cleanliness.

Opticap® XL 2, 4, 5 and 10 Capsule Filters Opticap® XL disposable capsule filters with hydrophilic Durapore® membrane are available in multiple filtration areas, providing an optimal choice for every application. The unique capsule design minimizes hold-up volume and reduces production losses.

Opticap® XLT 10, 20 and 30 Capsule Filters Opticap® XLT disposable T-line capsule filters with hydrophilic Durapore® membrane are available with or without a pressure gauge port for ease in monitoring process conditions. The T-line design accommodates series or parallel filtration to match your application needs, and a specially-designed stand enables quick and easy integration into your existing process.

Opticap® XL Filters

Opticap® XLT Filters

Opticap® XLT Capsule Filter Stand

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Specifications OptiScale® 25 Filters OptiScale® 47 Filters Millipak® 100 Filters Millipak® 200 Filters

Nominal Dimensions

Maximum length: 39 mm (1.52 in.) with female Luer-Lok™ inlet/ male luer slip outlet

82 mm (3.24 in.) with flange inlet/hose barb outlet;74 mm (2.91 in.) with flange inlet/flange outlet;94 mm (3.70 in.) with hose barb inlet/hose barb outlet

13 cm (5.1 in.) 15.5 cm (6.1 in.)

Body diameter: 31 mm (1.21 in.) 70 mm (2.75 in.) 7.6 cm (3.0 in.) 7.6 cm (3.0 in.)

Weight: 0.19 oz (5.5 g) 2.4 oz (69 g) — —

Filtration Area 3.5 cm2 17.7 cm2 500 cm2 (0.54 ft2) 1000 cm2 (1.08 ft2)

Materials of Construction

Filter membrane: Hydrophilic PVDF Hydrophilic PVDF Hydrophilic PVDF

Structural components: Polypropylene Polycarbonate Polycarbonate

Supports (when used): Polypropylene Polypropylene —

Vent caps: Polypropylene PVDF PVDF

Internal seal rings: — Fluoroelastomers —

Housing Vent Capped vent with female Luer connections on inlet side of device.

Adjustable vent with male Luer slip and female Luer-Lok™ connections on inlet side of device.

Maximum Inlet Pressure 4.1 bar (60 psi) at 25 °C 5.5 bar (80 psi) at 25 °C 5.2 bar (75 psi) at 25 °C

Maximum Differential Pressure

Forward: 4.1 bar (60 psi) at 25 °C 5.5 bar (80 psi) at 25 °C 4.1 bar (60 psi) at 25°C

Reverse: 0 psi at 25 °C 0.7 bar (10 psi) at 25 °C 0.7 bar (10 psi) at 25 °C

Bubble Point at 23 °C

0.1 µm: — — ≥ 4830 mbar (70.0 psig) air with water

0.22 µm: — — ≥ 3450 mbar (50.0 psig) air with water

NVR Gravimetric Extractables — — After autoclaving and a 24 hour soak in ASTM®Type 1 reagent grade water at controlled room temperature:

≤ 2.5 mg ≤ 5.0 mg

Oxidizable Substances — Meets the requirements of USP Oxidizable Substances Test after a water flush of:

100 mL 200 mL 200 mL

Bacterial Endotoxin Aqueous extraction contains

5

Specifications (continued) Opticap® XL 2 Filters Opticap® XL 4 Filters Opticap® XL 5 Filters Opticap® XL 10 Filters

Nominal Dimensions

Maximum length: 14.2 cm (5.6 in.) 19.6 cm (7.7 in.) 21.6 cm (8.5 in.) 33.5 cm (13.2 in.)

Body diameter: 8.4 cm (3.3 in.) 8.4 cm (3.3 in.) 10.7 cm (4.2 in.) 10.7 cm (4.2 in.)

Filtration Area 0.09 m2 (0.93 ft2) 0.19 m2 (2.09 ft2) 0.34 m²(3.7 ft2) 0.69 m2 (7.4 ft2)

Materials of Construction

Filter membrane: Hydrophilic PVDF

Film edge: Polypropylene

Supports: Polypropylene

Structural components*: Polypropylene

Vent O-rings: Silicone

Vent/Drain ¼ in. hose barb with double O-ring seal

Maximum Inlet Pressure 5.5 bar (80 psi) at 23 °C2.8 bar (40 psi) at 60 °C1.0 bar (15 psi) at 80 °C

Maximum Differential Pressure

Forward: 5.5 bar (80 psid) at 25 °C, 1.0 bar (15 psid) at 80 °C

Reverse: 3.4 bar (50 psid) at 25 °C, intermittent

Bubble Point at 23 °C

0.1 µm: ≥ 4830 mbar (70.0 psig) air with water

0.22 µm: ≥ 3450 mbar (50.0 psig) air with water

Air Diffusion Through a water wet membrane at ambient temperature:

0.1 µm at 3.9 bar (56 psig): — ≤ 7.5 cc/min ≤ 10.0 cc/min ≤ 20.0 cc/min

0.22 µm of 2.8 bar (40 psig): — ≤ 5.5 cc/min ≤ 6.6 cc/min ≤ 13.3 cc/min

NVR Gravimetric Extractables After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:

≤ 10 mg ≤ 10 mg ≤ 15 mg ≤ 25 mg

Oxidizable Substances Meets the requirements of the USP Oxidizable Substances Test after a water flush of:

500 mL 500 mL 500 mL 1000 mL

Bacterial Endotoxin Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.

Bacterial Retention Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.

Sterilization May be autoclaved for 3 cycles of 60 minutes at 126 °C. (Cannot be steam sterilized in-line.)

Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Non-Fiber Releasing Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).

Component Material Toxicity Component materials were tested and meet the criteria of the USP Reactivity Test for Class VI Plastics. Sterilizing-grade Durapore® filters meet the requirements of the current USP Safety Test.

Indirect Food Additive The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910. All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177–182.

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Specifications (continued) Opticap® XLT 10 Filters Opticap® XLT 20 Filters Opticap® XLT 30 Filters

Nominal Dimensions

Maximum length: 38.1 cm (15.0 in) 62.5 cm (24.6 in.) 87.1 cm (34.3 in.)

Fitting to Fitting

Sanitary flange to sanitary flange: 15.2 cm (6.0 in.) 15.2 cm (6.0 in.) 15.2 cm (6.0 in.)

Sanitary flange to hose barb: 17.5 cm (6.9 in.) 17.5 cm (6.9 in.) 17.5 cm (6.9 in.)

Hose barb to hose barb: 19.8 cm (7.8 in.) 19.8 cm (7.8 in.) 19.8 cm (7.8 in.)

Filtration Area 0.69 m2 (7.4 ft2) 1.4 m2 (14.8 ft2) 2.1 m2 (22.2 ft2)

Materials of Construction

Filter membrane: Hydrophilic PVDF

Film edge: Polypropylene

Supports: Polypropylene

Structural components*: Polypropylene

Vent O-rings: Silicone

Maximum Inlet Pressure 5.5 bar (80 psi) at 23 °C

2.8 bar (40 psi) at 60 °C

1.0 bar (15 psi) at 80 °C

Maximum Differential Pressure

Forward: 5.5 bar (80 psid) at 25 °C, 1.7 bar (25 psid) at 80 °C

Reverse: 3.4 bar (50 psid) at 25°C

Bubble Point at 23 °C

0.1 µm: ≥ 4830 mbar (70.0 psig) air with water

0.22 µm: ≥ 3450 mbar (50.0 psig) air with water

Air Diffusion Through a water wet membrane at ambient temperature:

0.1 µm at 3.9 bar (56 psig): ≤ 20.0 cc/min ≤ 40.0 cc/min ≤ 60.0 cc/min

0.22 µm of 2.8 bar (40 psig): ≤ 13.3 cc/min ≤ 26.6 cc/min ≤ 39.9 cc/min

NVR Gravimetric Extractables After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:

≤ 25 mg ≤ 50 mg ≤ 75 mg

Oxidizable Substances Meets the requirements of the USP Oxidizable Substances Test after a water flush of:

1000 mL 2000 mL 3000 mL

Bacterial Endotoxin Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.

Bacterial Retention Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.

Sterilization May be autoclaved for 3 cycles of 60 minutes at 126 °C. (Cannot be steam sterilized in-line.)

Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Non-Fiber Releasing Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).

Component Material Toxicity Component materials were tested and meet the criteria of the USP Reactivity Test for Class VI Plastics. Sterilizing-grade Durapore® filters meet the requirements of the current USP Safety Test.

Indirect Food Additive The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910. All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182.

*Cage, core, end caps and capsule housing

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Specifications (continued) 5-inch Cartridge Per 10-inch Cartridge

Nominal Dimensions

Outside diameter: 6.9 cm (2.7 in.) 6.9 cm (2.7 in.)

Filtration Area 0.35 m2 (3.8 ft²) 0.69 m2 (7.4 ft2)

Materials of Construction

Filter membrane: Hydrophilic PVDF

Film edge: Polypropylene

Supports: Polypropylene

Structural components: Polypropylene

O-rings: Silicone

Maximum Differential Pressure

Forward: 5.5 bar (80 psid) at 25 °C, 1.7 bar (25 psid) at 80 °C, 345 mbar (5 psid) at 135 °C

Reverse: 3.4 bar (50 psid) at 25 °C, intermittent

Bubble Point at 23 °C

0.1 µm: ≥ 4830 mbar (70.0 psig) air with water

0.22 µm: ≥ 3450 mbar (50.0 psig) air with water

Air Diffusion Through a water wet membrane at ambient temperature:

0.1 µm at 3.9 bar (56 psig): ≤ 10 cc/min ≤ 20.0 cc/min

0.22 µm of 2.8 bar (40 psig): ≤ 6.6 cc/min ≤ 13.3 cc/min

NVR Gravimetric Extractables After autoclaving and a 24 hour soak in ASTM® Type 1 reagent grade water at controlled room temperature:

≤ 10 mg ≤ 20 mg

Oxidizable Substances Meets the requirements of the USP Oxidizable Substances Test after a water flush of:≤1000 mL per 10-inch element

Bacterial Endotoxin Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.

Bacterial Retention Quantitative retention of 107 CFU/cm2 Brevundimonas diminuta ATCC® 19146 per ASTM® methodology.

Sterilization May be autoclaved for 30 cycles of 60 minutes at 126 °C or steam sterilized up to 30 times for 30 minutes at 135 °C.

Good Manufacturing Practices These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

Non-Fiber Releasing Durapore® membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).

Component Material Toxicity Component materials were tested and meet the criteria of the USP Reactivity Test for Class VI Plastics. Sterilizing-grade Durapore® filters meet the requirements of the current USP Safety Test.

Indirect Food Additive The Durapore® membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910. All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177–182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.

Total Organic Carbon (TOC) and Conductivity

0.1 µm: Device effluent met the TOC acceptance criteria per USP and the conductivity acceptance criteria per USP after autoclaving with a WFI water flush of 3.5 L per ten-inch cartridge.

0.22 µm: Device effluent met the TOC acceptance criteria per USP and the conductivity acceptance criteria per USP after autoclaving with a WFI water flush of 5.5 L per ten-inch cartridge.

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Typical Clean Water Flow RatesMillipak® Capsule FiltersMillipak® 100/200 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XL Capsule FiltersOpticap® XL 2 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XL 4 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XL 10 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

A = 14 mm (9/16 in.) Hose Barb Inlet and Outlet

B = 6 mm (¼ in.) NPTM Inlet and Outlet

F = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet

L = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

Opticap® XL Capsule Legends Refer to Connection Type

TT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

FF = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet

HH = 14 mm (9/16 in.) Hose Barb Inlet and Outlet

TH = 38 mm (1½ in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet

FH = 19 mm (¾ in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet (XL 2 and 4 only)

Millipak® 100/200 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XL 5 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XL 10 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XL 4 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XL 5 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XL 2 Capsule Filters —0.22 µm Hydrophilic Durapore® Membrane

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Opticap® XLT Capsule FiltersOpticap® XLT 10 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XLT 20 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XLT 30 Capsule Filters — 0.1 µm Hydrophilic Durapore® Membrane

Cartridge FiltersCartridge Filters — 0.1 µm Hydrophilic Durapore® Membrane

Opticap® XLT 10 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XLT 20 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XLT 30 Capsule Filters — 0.22 µm Hydrophilic Durapore® Membrane

Cartridge Filters — 0.22 µm Hydrophilic Durapore® Membrane

Opticap® XLT Capsule Legends Refer to Connection Type

TT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

TH = 38 mm (1½ in.) Sanitary Flange Inlet and 16 mm (5/8 in.) Hose Barb Outlet

HH = 16 mm (5/8 in.) Hose Barb Inlet and OutletBB = 25 mm (1 in.) Hose Barb Inlet and Outlet

Typical Clean Water Flow Rates

10

OptiScale® Capsule Filters

Ordering Information

Millipak® Capsule Filters

Opticap® XL Capsule Filters*

S V A

OptiScale® Capsule Filter

Membrane TypeV = Durapore®

Pore SizeVL = 0.1 µmGL = 0.22 µm

Disc Size25 = 25 mm47 = 47 mm

Quantity per Package3 = 3/pk6 = 6/pk

Connection TypeHH = 6 mm (¼ in.) Hose Barb Inlet and Outlet

FF = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet

FH = 19 mm (¾ in.) Sanitary Flange Inlet and 6 mm (¼ in.) Hose Barb Outlet

NB = Female Luer-Lok™ Inlet/Male Luer Slip Outlet

May be Autoclaved

Millipak® Capsule Filter

Membrane Pore SizeVL = Durapore® 0.1 µmGL = Durapore® 0.22 µm

Millipak® Cartridge Filter Series10C = Millipak® 100, Non-sterile20C = Millipak® 200, Non-sterile

Quantity per Package3 = 3/pk

Connection TypeA = 14 mm (9/16 in.) Hose Barb and Outlet

B = 6 mm (¼ in.) NPTM and Outlet

F = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet

L = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

M P 3

K V A

Opticap® XL Capsule Filter

Membrane TypeV = Durapore®

Pore SizeVL = 0.1 µmGL = 0.22 µm

Capsule Size02 = Opticap® XL 2 04 = Opticap® XL 4 05 = Opticap® XL 510 = Opticap® XL 10

Quantity per Package1 = 1/pk

(Opticap® XL 5 and 10 filters only)3 = 3/pk

(Opticap® XL 2 and 4 filters only)

Connection TypeTT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

FF = 19 mm (¾ in.) Sanitary Flange Inlet and Outlet

HH = 14 mm (9/16 in.) Hose Barb Inlet and Outlet

TH = 38 mm (1½ in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet

FH = 19 mm (¾ in.) Sanitary Flange Inlet and 14 mm (9/16 in.) Hose Barb Outlet (Opticap® XL 2 and 4 filters only)

NN = 6 mm (¼ in.) NPT Inlet and Outlet (Opticap® XL 2 and 4 filters only, 0.22 um only)

May be Autoclaved

11

Cartridge Code 0 = (2-222) O-ring 5 = (2-222) O-ring w/spear 7 = (2-226) O-ring with

locking tab and spear

Standard Opticap® XLT Capsule Filter Stand 1 XLTSTAND1

Opticap® XLT Capsule Filters*

Ordering Information

Cartridge Filters

K V A

Opticap® XLT Capsule Filter

Membrane TypeV = Durapore®

Pore SizeVL = 0.1 µmGL = 0.22 µm

Gauge PortT = Without Gauge

PortZ = With Gauge

Port

Capsule Size1 = Opticap® XLT 102 = Opticap® XLT 203 = Opticap® XLT 30

Quantity per Package1 = 1/pk

Connection TypeTT = 38 mm (1½ in.) Sanitary Flange Inlet and Outlet

HH = 16 mm (5/8 in.) Hose Barb Inlet and Outlet

TH = 38 mm (1½ in.) Sanitary Flange Inlet and 16 mm (5/8 in.) Hose Barb Outlet

BB = 25 mm (1 in.) Hose Barb Inlet and Outlet

May be Autoclaved

1

*Not all configurations available as standard product.

Discription Qty/pk Catalogue no.

C V

Cartridge Filter

Membrane TypeV = Durapore®

Pore SizeVL = 0.1 µmGL = 0.22 µm

Cartridge Length1 = 10 inch 2 = 20 inch 3 = 30 inch5 = 5 inch

(Code 0 and Code 7 only)

Packaging CodeS01 = 1/pk (5-inch element only)TP3 = 3/pk (all other elements)

EMD Millipore, the M logo, Durapore, Millipak, Opticap, and OptiScale are registered trademarks of Merck KGaA, Darmstadt, Germany. ISO is a registered trademark of the International Organization for Standardization. ASTM is a registered trademark of American Society for Testing and Materials. ATCC is a registered trademark of American Type Culture Collection. Luer-Lok is a trademark of Becton Dickinson and Company. Lit No. DS160EN00 Rev. H 06/2015 DP-SBU-11-04815 © 2015 EMD Millipore Corporation, Billerica, MA, USA. All rights reserved.

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