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Filter NRFit

Pajunk GmbH Medizintechnologie · Model 001163-39F · UDI-DI 14048223041793

BSN Prescription
1
510(k) clearances
163
Adverse events
1
Recalls
17
Facilities

Description

Filter NRFit

Recalls

DateFirmReason
2009-11-25Millipore CorporationMembrane integrity defects may allow the passage of viable or non-viable contaminants to pass through the filter.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.