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RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 230-330-018 · UDI-DI 04049197150583

KAI Prescription
9
510(k) clearances
4
Adverse events
1
Recalls
109
Facilities

Description

Larynx Mirror Fig. 4 180mm, 7", Ø 18mm with hexagonal handle

Recalls

DateFirmReason
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

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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.