BEUDAMED
    33 results · 23ms · Sources: EU EUDAMED, US FDA

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    Versana Premier

    FDA 510(k)
    FDA Class 2 ·Radiology

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780454632·Integra® Jarit® Crile Retractor, 4-1/4", Double...

    TREGOR®

    FDA UDI
    ASTON MEDICAL·03663703000387·Reinforcement device

    GERALD TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060180·GERALD FORCEPS TUNGSTEN CARBIDE DUST

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306804984·Cerkes Micro Osteotome, 4mm

    Initia Total Hip System

    FDA UDI
    KYOCERA CORPORATION·04547898307317·STDHO LINER 32-60/64

    Initia Total Hip System

    FDA UDI
    KYOCERA MEDICAL CORPORATION·04580810058072·"STDHO LINER 32-56/58 Size:32-56/58 Type:Flat, ...

    EZout

    FDA UDI
    STRYKER CORPORATION·07613327176070·Riser Ring, 38-40mm

    Minuteman

    FDA UDI
    Spinal Simplicity, LLC·M9432001380000·Weitlaner Retractor 16.5cm

    NA

    FDA UDI
    aap Implantate AG·04042409080104·Cortical Screw 2.0, L 38

    STAT-SITE MHGB METER, STAT-SITE MHGB METER CARD HOLDER, STAT-SITE MHGB TEST CARDS, STAT-SITE MHGB CODE WAY, MODELS 90090

    FDA 510(k)
    FDA Class 2 ·Hematology

    MIDAS TOUCH NITRILE EXAMINATION GLOVES-POWDERFREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 10, 2002

    NA

    FDA UDI
    aap Implantate AG·04042409080111·Cortical Screw 2.0, L 38

    G-PROBE RFID

    FDA Adverse Event
    Malfunction ·IRIDEX CORPORATION·Product code GEX·April 4, 2023

    SUBCHONDROPLASTY

    FDA Adverse Event
    Injury ·ZIMMER KNEE CREATIONS, INC.·Product code OJH·October 22, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 6, 2023

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008

    ECHELON 60 ENDOPATH

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 1, 2013