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ERGOPERIO

Aesculap AG · Model DX071R · UDI-DI 04046964540103

EMG Prescription
10
510(k) clearances
11
Adverse events
1
Recalls
215
Facilities

Description

ERGOPERIO Micro Forceps, curved, 6 7/8", (175 mm), toothing DE BAKEY, non-sterile, reusable

Recalls

DateFirmReason
2008-05-21Biomet Microfixation, Inc.The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997.

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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.