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Merck
CN

SAU0200L41DP5

Mobius® Silver Drum Assembly

200L Standard PureFlex™ Drum Assembly

Synonym(s):

Mobius®, Silver, 200 L Standard PureFlex™ Drum Assembly

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About This Item

eCl@ss:
32031690
UNSPSC Code:
23151806

Key Documents

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Technical Service
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material

PureFlex™ container, PureFlex™ film

Quality Level

400

sterility

sterile; γ-irradiated (Sterilized using a validated gamma irradiation level of 25-40 kGy)

product line

EMPROVE® Single Use, Mobius®

parameter

200 L sample volume

fitting

(1/2 in. MPX Coupling Body, 1/2 in. MPX Sealing Plug, Pinch Clamp, Cable Tie)

application(s)

pharmaceutical

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General description

Mobius® standard drum assemblies are reliable, ready-to-use fluid storage and processing solutions for biopharmaceutical applications. These convenient single-use systems feature pre-sterilized PureFlex™ film containers available in 50 L to 200 L volumes. Designed to fit Mobius® polyethylene drums and other commercial storage drums, these assemblies minimize operator error and process risks while maximizing operational efficiency in bioprocessing workflows.

Application

Mobius® standard drum assemblies are ideal for buffer storage, media preparation, intermediate product holding, and general fluid transfer operations in biopharmaceutical manufacturing processes.

Features and Benefits

  • Flexible
  • Easy to set up and use
  • Mobius® Silver Certification
  • Sterilized using gamma irradiation
  • Excellent gas barrier performance

Legal Information

Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
MOBIUS is a registered trademark of Merck KGaA, Darmstadt, Germany
PUREFLEX is a trademark of Merck KGaA, Darmstadt, Germany

Certificates of Analysis (COA)

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Articles

Best Practices for Qualifying Single-Use Assemblies

Key aspects of single-use assembly qualification including quality by design (QbD), quality risk management (QRM) and operator handling and training.

Extractables and Leachables Risk Assessment for Single-Use Systems

Before adoption of single-use technologies in biomanufacturing, manufacturers must assess the risk to the drug product from potential leachables. This article highlights a general approach based on the United States Pharmacopeia (USP).

Reducing the Need for Animal Testing for Biological Reactivity in Polymer Characterization

This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.

Building Regional Single-Use Supply Chains

Our global network of raw material suppliers and regional production sites for single-use technologies ensures business continuity for biopharma customers.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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