BEUDAMED
    919 results · 22ms · Sources: EU EUDAMED, US FDA

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    Intess L

    FDA UDI
    Kalitec Direct LLC·B07312K0100310·Assembly,Caddie, Lumbar Implants, Hinged

    Matira

    FDA UDI
    Kalitec Direct LLC·B073DRK010031·Drill Guide, Straight, Featureless, Amann

    Inseption

    FDA UDI
    Kalitec Direct LLC·B07314K0100310·Assembly, Caddie, ISP Implants, Hinged

    NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Armstrong

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490028110·VENT TUBE 1010031 50PK ARMSTR BEV GROM

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964054264·Endo Carry-on Procedure Kit Includes Basin, Enz...

    Armstrong

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000038472·VENT TUBE 1010031 50PK ARMSTR BEV GROM

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10884389002056·CIRCUIT-ADULT ANESTHESIA

    MIS T25 SUPER LOCKING DRIVER

    FDA UDI
    Osteocentric Technologies, Inc.·00810097802469·MIS T25 SUPER LOCKING DRIVER

    Elite Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7403010031·16mm Paddle Distractor

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10884389000687·CIRCUIT-ADULT ANESTHESIA

    AQUANET, MODEL EC 2000

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

    URANUS, COMFORTOUCH LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POLY-TAPE, 20 X 500MM

    FDA Adverse Event
    Injury ·XIROS·Product code JDR·December 6, 2011

    EQUINOXE

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code KWT·May 31, 2023

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·March 2, 2011

    BIODESIGN URETHRAL SLING

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code FTM·July 29, 2013

    Endotec Prothesis Ankle, Titanium Alloy, Sterilized, BP Ankle System. BP Ankle System, F-P Type III Ankle Bearing Component: 2x5mm F-P Type III Ankle Bearing Catalog: 05-13-0532, 2x7mm F-P Type III Ankle Bearing Catalog: 05-13-0732, 8x3mm F-P Type III Ankle Bearing Catalog: 05-13-0533, 8x1mm F-P Type III Ankle Bearing Catalog: 05-13-0731. BP Ankle System, F-P Type III Tibial Ankle Component: Size 1 F-P Type III Tibial Component Catalog: 05-12-0031, Size 2 F-P Type III Tibial Component Catalog: 05-12-0032, Size 3 F-P Type III Tibial Component Catalog: 05-12-0033. BP Ankle System, F-P Type III Talar Component: Size 1 F-P Type III Talar Component Catalog: 05-01-0031, Size 2 F-P Type III Talar Component Catalog: 05-01-0032, Size 3 F-P Type III Talar Component Catalog: 05-01-0033.

    FDA Recall
    Terminated ·Endotec, Inc.·Product code JWH·June 5, 2009