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Ameda, Inc.

AMEDA, INC. · Model 17141 · UDI-DI 00810725020548

HGY
1
510(k) clearances
82
Adverse events
2
Recalls
92
Facilities

Description

One-Hand Pump HygieniKit Adapter (STL)

Recalls

DateFirmReason
2015-02-12Ameda, Inc.Devices were not sterilized
2015-02-12Ameda, Inc.Devices were not sterilized

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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.