BEUDAMED
    29 results · 23ms · 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 ×

    RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CompCORE AF

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783000719·COMPCORE AF DUAL CURE WHITE INTRO KIT

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092165973·Straumann® BL RC-compatible Engaging Verificati...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001430·artVeneer life upper anteriors, CM, D2

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00143021·

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092125724·Straumann® BL RC-compatible Engaging Verificati...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008453·PedFuse Respond, CNL, 7.0mm x 30mm

    AFFINITY NT HOLLOW FIBER OXYGENATOR WITH PLASMA RESISTANT FIBER WITH CARMEDA BIOACTIVE SURFACE, MODEL CB511

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    ATTAIN LV

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·February 3, 2016

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    STANDARD TPLO JIG FOR USE W/ 24MM/27MM/30MM SAW GUIDES

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code FZX·March 13, 2013

    PUMP, INFUSION, ELASTOMERIC

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 25, 2011

    INTEGRA NEUROSCIENCES HERMETIC LUMBAR CATHETER CLOSED

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES·Product code JXG·February 19, 2008