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RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 250-052-000 · UDI-DI 04049197390743

EQH Prescription
10
510(k) clearances
36
Adverse events
1
Recalls
99
Facilities

Description

Adaptor f. Fiberlight cable, HEINE facing to the unit

Recalls

DateFirmReason
2007-02-07Boston Scientific CorporationLight Degradation in transmission-A film may deposit on the front face and limit transmission of light

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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.