BEUDAMED
    24 results · 21ms · 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 ×

    SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Safco T&F Bur - 12 Bladed

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310220653·Safco T&F bur - 12 bladed, carbide, #7406 egg F...

    nSpire Health

    FDA UDI
    NSPIRE HEALTH, INC.·10852417003696·KoKo Standard White Filter Kit with Nose Clip a...

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120220651·Carbide, flame, fine finishing bur, yellow ring

    OCTOSTOP, INC.

    FDA registration
    OCTOSTOP, INC.·4 products·🇨🇦 Canada

    AOS CANCELLOUS SCREW 5.0mm x 65.0mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665020106·

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967162317·ANGLED THORACIC SUPRALAMINAR HOOK, LEFT, 6.5mm

    LINK Instruments - Trial implants and size gauges

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575409150·Acetabulum prosthesis trial, reusable - Vario-C...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197256469·Chelsea Eaton Anuscope 22x65mm

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197393003·Tilley Henckel Ethmoid Punch Ø6.5mm...

    PATIENT LATEX POLYMER COATED POWDER-FREE GLOVES, CONTAINS 50 MICROGRAM OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    WIENER LAB. CREATININA CINETICA AA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967160160·22° OFFSET TRANSVERSE PROCESS HOOK, LEFT, 6.5mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967160702·NARROW BLADE 22° OFFSET TRANSVERSE PROCESS HOOK...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967160528·22° OFFSET TRANSVERSE PROCESS HOOK, RIGHT, 6.5mm

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967160344·NARROW BLADE 22° OFFSET TRANSVERSE PROCESS HOOK...

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·March 26, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 10, 2011

    BD PARADIGM LINK GLUCOSE MONITOR

    FDA Adverse Event
    Malfunction ·NOVA BIOMEDICAL CORP.·Product code NBW·March 28, 2008

    Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An electrically-powered device intended to provide suitable warming and/or incubation conditions for reproductive biological materials (e.g., gametes and embryos), at closely regulated and monitored temperatures, during assisted reproduction examination and processing procedures. It may support a more comprehensive growth environment [e.g., temperature, carbon dioxide (CO2) and oxygen (O2) concentration]; it typically has adjustment and monitoring controls. Component: N/A

    FDA Recall
    Open, Classified ·CooperSurgical, Inc.·Product code PUB·November 15, 2024