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mahe medical GmbH

mahe medical gmbh · Model 35.007.20 · UDI-DI 04050659368293

JFL
10
510(k) clearances
3
Adverse events
3
Recalls
15
Facilities

Description

Cysto.-Urethro.-sheath,compl.,25Ch. _x000D_for 4.0mm optic _x000D_

Recalls

DateFirmReason
2020-01-29Beckman Coulter Inc.Electrolyte reference reagent, used for clinical laboratory testing to determine CO2 in human serum or plasma for diagnosis and treatment of potentially serious disorders associate
2004-09-08Hospira IncThe batteries in Plum A+ and Plum A+3 I.V. infusion pumps may fail prematurely when the pump is operating solely on battery power.
2004-09-08Hospira IncThe batteries in Plum A+ and Plum A+3 I.V. infusion pumps may fail prematurely when the pump is operating solely on battery power.

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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.