BEUDAMED
    22 results · 30ms · 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 ×

    Brightway Brand Nitrile Examination Gloves, Powder Free, [Sterling/Grey] Tested For Use With Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK112151·DD tempMED are pre-colored dental milling blank...

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071102005·16FR x 1.2 cm x 15 cm Low Profile Transgastric-...

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071134525·16FR x 1.2 cm x 15 cm Low Profile Transgastric-...

    NUANCE

    FDA 510(k)
    FDA Class 2 ·Dental

    VOLCANO S51 FAMILY OF IMAGING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071117016·16FR x 1.2 cm x 15 cm Low Profile Transgastric-...

    G-Jet® Transgastric-Jejunal Feeding Device

    FDA UDI
    APPLIED MEDICAL TECHNOLOGY, INC.·00842071134532·16FR x 1.2 cm x 15 cm Low Profile Transgastric-...

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·April 22, 2019

    EXPRESSEW III AC+ GUN

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL·Product code LXH·November 25, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 13, 2011

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 15, 2008

    DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·March 23, 2018

    Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 16CM (0.021), REF/Product Code RM*RS7F16PA, STERILE, Rx ONLY

    FDA Enforcement
    Class II ·Terminated·Terumo Medical Corp·December 20, 2017

    Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit, 6FR - 10CM (0.021), REF/Product Code RM*ES6F10HAU, STERILE, Rx ONLY

    FDA Enforcement
    Class II ·Terminated·Terumo Medical Corp·December 20, 2017