BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    MANUAL PHENYLALANINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111161·FOX EYE SHIELD GARTERS WHITE PACK OF 50

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197077453·Ribbon Retractor 40 x 3...

    DISPOSABLE INTRAVENOUS HYPERALIMENTATION BAGS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    A-1103 ABUTMENT (REMOVABLE)

    FDA 510(k)
    FDA Class 2 ·Dental

    RINGLOC+ REPLACEMENT RING SZ21

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·April 27, 2018

    E1 44-36 STD HMRL BRNG

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PAO·April 27, 2018

    WIRE COLLET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·January 24, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 18, 2011

    RENASYS GO POWER SUPPLY

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW WOUND MANAGEMENT·Product code BTA·July 29, 2014

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026