BEUDAMED
    27 results · 22ms · 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 ×

    POWDER FREE NITRILE EXAMINATION GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUGS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ANA 70 Capsules 2 Spill 50 count

    FDA UDI
    Wykle Research, Inc·00853383006875·

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664131005·FOR MEN CASUAL 15-20 MM HG KNEE HIGH CLOSED TOE...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702867930·ELVAREX 1/KNEE HIGH/SLANT-CLOSED TOE/DOTTED SIL...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702597721·ELVAREX 2/KNEE HIGH/PROFILE-SLANT-CLOSED TOE/SO...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702256772·ELVAREX 2/THIGH HIGH/SLANT, OPEN TOE, E-VERSION...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702557039·Elvarex 3/Knee High/Slant-Closed Toe-Elephantia...

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122209·KWire .045x4" (1.1x100mm)

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642104127·Rod Curved 5.5 x 100mm

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315818590·XL t(14;18) IGH/BCL2 DF, Translocation/Dual Fus...

    MOUNTAINEER OCT SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROPOXYPHENE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123919·CR Femoral Trial Sz 1 L

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142712·L PS Cemented Femoral Component Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147915·PS Femoral Trial Sz 1 L

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197398169·XL Rainer Cervical Microdiscectomy Curett...

    DELTA CERAMIC FEM HD 36/+6MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 15, 2026

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 28, 2014

    PLUM A + DRIVER NEW

    FDA Adverse Event
    Malfunction ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·May 9, 2013

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 20, 2011