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RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 350-843-210 · UDI-DI 04049197272575

HFB Prescription
10
510(k) clearances
60
Adverse events
1
Recalls
164
Facilities

Description

Faure biopsy forceps 21 cm, 8 1/4 "

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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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.