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FILTER
Pajunk GmbH Medizintechnologie · Model 001163-39F · UDI-DI 04048223050064
1
510(k) clearances
162
Adverse events
1
Recalls
18
Facilities
Description
001163-39F
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-11-25 | Millipore Corporation | Membrane integrity defects may allow the passage of viable or non-viable contaminants to pass through the filter. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.