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Fresenius

Fresenius Medical Care Holdings, Inc. · Model 04-9500-2 · UDI-DI 10840861100542

FIB
1
510(k) clearances
41
Adverse events
0
Recalls
20
Facilities

Description

Transducer Protectors, bulk pack

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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.