BEUDAMED
    27 results · 26ms · 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 ×

    ONE STEP MULTIPLE DRUGS OF ABUSE ASSAYS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    EASYLIFE

    FDA UDI
    Respironics, Inc.·00606959001329·Large EasyLife Mask with Headgear, China

    Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989025354·PREF.LING.ARCH NI-TI UP18 SZ2 PK/10

    Humelock II Cemented Reversible Shoulder

    FDA UDI
    FX SOLUTIONS·03701037300237·HUMELOCK REVERSED TA6V CEMENTLESS GLENOID BASEP...

    Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW

    FDA UDI
    Osteocentric Technologies, Inc.·00816950026690·Ø7.0 x 24mm x 50mm CANNULATED PARTIAL THREAD SCREW

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·CRYOCOR CRYOABLATION SYSTEM

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710300500240·Tibial Osteotmy Guide, 50mm x 24mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420500240·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710400500240·Anterior Dome Osteotomy Guide, 50mm x 24mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410500240·Anterior Closing Wedge Osteotomy Guide, 50mm x ...

    CARIS MINITOME BIOPSY INSTRUMENT

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

    O2/CO2 NASAL FILTERLINE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·CRYOCOR CRYOABLATION SYSTEM

    HUMELOCK REVERSED SHOULDER

    FDA Adverse Event
    Injury ·FX SOLUTIONS·Product code PHX·June 21, 2019

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013

    HUMELOCK REVERSED SHOULDER

    FDA Adverse Event
    Injury ·FX SOLUTIONS·Product code PHX·July 9, 2019

    TGS UKA KNEE SYSTEM

    FDA Adverse Event
    Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·CAYENNE MEDICAL INC.·Product code HSX·May 15, 2014