BEUDAMED
    2,536 results · 39ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Dandy Scan Body

    FDA UDI
    Coremedtech ApS·05744003810703·Dandy Scan Body, by CoreMedTech, for dental Int...

    UNKNOWN EMPRINT ANTENNA

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NEY·February 17, 2026

    UNK_ECHELON CIRCULAR POWERED STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 20, 2022

    ECHELON FLEX 60 POWERED PLUS ENDOPATH STAPLER ARTICULATING ENDOSCOPIC LINEAR CUT

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 2, 2023

    ZUK PRC FEM SZB RMED/LLAT¿ ZUK PRC FEM SZC LMED/RLAT¿ ZUK PRC FEM SZC RMED/LLAT¿ NGU PRC FEM SZD LMED/RLAT¿ ZUK PRC FEM SZD RMED/LLAT¿ ZUK PRC FEM SZE LMED/RLAT ZUK PRC FEM SZF RMED/LLAT " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. " These devices are indicated for cemented use only. " The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·March 21, 2018

    ZUK PRC FEM SZB RMED/LLAT ZUK PRC FEM SZC LMED/RLAT ZUK PRC FEM SZC RMED/LLAT NGU PRC FEM SZD LMED/RLAT ZUK PRC FEM SZD RMED/LLAT ZUK PRC FEM SZE LMED/RLAT ZUK PRC FEM SZF RMED/LLAT " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. " These devices are indicated for cemented use only. " The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code HSX·November 29, 2017

    Balloon, Liver Tamponade

    FDA classification
    FDA Class 2 ·Balloon, Liver Tamponade

    NAU S.P.A.

    FDA registration
    NAU S.P.A.·3 products·🇮🇹 Italy

    HARTALEGA NGC SDN BHD

    FDA registration
    HARTALEGA NGC SDN BHD·7 products·🇲🇾 Malaysia

    HARTALEGA NGC SDN. BHD. (LOT 39496)

    FDA registration
    HARTALEGA NGC SDN. BHD. (LOT 39496)·7 products·🇲🇾 Malaysia

    POPLOK

    FDA UDI
    Conmed Corporation·10845854030349·POPLOK DRILL GUIDE

    APS Dry Needling Neeedles

    FDA UDI
    AGU PUNT SL·08437016482162·

    AGUPUNT IPEN

    FDA UDI
    AGU PUNT SL·08437016482285·Physiotherapy needles

    AGUPUNT IPEN

    FDA UDI
    AGU PUNT SL·08437016482308·Physiotherapy needles

    AGUPUNT APS

    FDA UDI
    AGU PUNT SL·08437016482612·Physiotherapy needles

    AGUPUNT APS

    FDA UDI
    AGU PUNT SL·08437016482414·Physiotherapy needles

    APS Dry Needling Neeedles

    FDA UDI
    AGU PUNT SL·08437016482087·

    APS Dry Needling Neeedles

    FDA UDI
    AGU PUNT SL·08437016482995·Physiotherapy needles

    AGUPUNT IPEN

    FDA UDI
    AGU PUNT SL·08437016482315·Physiotherapy needles

    APS Dry Needling Neeedles

    FDA UDI
    AGU PUNT SL·08437016482544·