FDA Device Intelligence
Home › mahe medical gmbh › mahe medical GmbH

mahe medical GmbH

mahe medical gmbh · Model 50.036.05 · UDI-DI 04050659388277

NBH
2
510(k) clearances
5,126
Adverse events
55
Recalls
296
Facilities

Description

Arthroscopy trocar,blunt,OD 4.2mm, _x000D_HIGH-FLOW,f.optics 4.0/176mm _x000D_

Recalls

DateFirmReason
2020-09-21Smith & Nephew, Inc.The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.