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MEDPOR CONTAIN

Stryker Leibinger GmbH & Co. KG · Model 81068 · UDI-DI 07613252084495

NPK Prescription
1
510(k) clearances
83
Adverse events
1
Recalls
24
Facilities

Description

MEDPOR¿ CONTAIN? Implant Sheet

Recalls

DateFirmReason
2017-03-01Inion Ltd.Aluminum pouch seal was noticed to be defective (slightly open).

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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.