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Safety Information

PCC030C01C

Millipore

Pellicon® Capsule with Ultracel® Membrane

pore size 30 kDa, C Screen, size 0.1 m2 , with AseptiQuik® G connectors

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UNSPSC Code:
41104903

material

EPDM rubber seal
PPO/PS blend (core)
PPO/PS blend housing
TPE seal
Ultracel® membrane
composite regenerated cellulose (CRC) membrane
epoxy adhesive
polyester screen
polypropylene screen
polyurethane adhesive

Quality Level

sterility

sterile; γ-irradiated

product line

Pellicon®

storage condition

room temperature (15-30°C)

parameter

4-8 L/min-m2 flow rate (Feed)
50 psi max. transmembrane pressure (3.5 bar) at 4-30 °C (Forward)
75 psi max. inlet pressure (5.1 bar) at 4-30 °C

technique(s)

ultrafiltration: suitable

L

41.1 cm (16.2 in.)

diam.

3.8 cm (1.5 in.)

filtration area

0.1 m2

screen size

, Type C screen (coarse screen)

size

0.1 m2 , with AseptiQuik® G connectors

volume

38 mL , in feed channel
68 mL , in permeate channel

impurities

≤5 ppm Meets TOC (in retentate effluent, after a WFI flush of 20 L/m2)

matrix

Ultracel®

pore size

30 kDa

pH range

2-13

fitting

inlet/outlet connection (Feed: AseptiQuik® G Connector)
inlet/outlet connection (Permeate: AseptiQuik® G Connector)
inlet/outlet connection (Retentate: AseptiQuik® G Connector)

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General description

The Pellicon® Capsule is the first of its kind -- a true single-use TFF device that comes ready to process in minutes. Self-contained, it employs an easy-to-use, holderless format and is supplied sterilized by irradiation.

Application

Concentration, Diafiltration, Buffer exchange, Protein purification

Features and Benefits

Plug ′n play, holderless design - easy to install, safe to remove
Gamma sterilized and preseravtive-free - ready to process in minutes
True single-use, self-contained capusle - fast, safe, and flexible batch turnaround
Proven Ultracel® membrane and C screen - high recovery, superior mass transfer, solvent resistance
Pellicon® TFF proven performance - true linear scalability within Pellicon® TFF families

Packaging

A foam pouch is inserted over the end caps on both ends of the capsule which is then double-bagged and vacuum sealed. The double-bagged capsule is then placed on a tray and individually boxed.

Other Notes

The Emprove® Program complements the product portfolio through

Comprehensive documentation to support qualification, risk assessment and process optimization needs.
Consolidation of product specific testing, quality and regulatory information to simplify compliance requirements.
Convenient 24/7 access to up-to-date product information.

Legal Information

AseptiQuik is a registered trademark of Colder Products Company
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
Pellicon is a registered trademark of Merck KGaA, Darmstadt, Germany
ULTRACEL is a registered trademark of Merck KGaA, Darmstadt, Germany

Regulatory Information

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Articles

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