BEUDAMED
    73 results · 30ms · Sources: EU EUDAMED, US FDA

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    WU'S POWERED WHEELCHAIR, MAMBO 36X

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    External thermoplastic nasal splint

    FDA UDI
    Spiggle & Theis Medizintechnik GmbH·04250381809969·100x75 mm, cuttable, 2.4 mm 10 pie...

    Liko™ M220 mobile lift

    FDA UDI
    Liko AB·00887761981898·Mobile patient lifting system, battery-powered

    Humelock II Cemented Reversible Shoulder

    FDA UDI
    FX SOLUTIONS·03701037300220·POST EXTENSION TA6V +10 mm CEMENTLESS Ti/HA

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948011104·SILVERVENT 1 ICU, SIZE 10

    Ni-Ti - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989025255·PREF ARCH NI-TI UPPER 14 LARGE PK10

    OSE

    FDA UDI
    ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042120037·Neet™ Nickel Titanium Molar Separating Springs

    BECKMAN COULTER, INC.

    FDA registration
    BECKMAN COULTER, INC.·120 products·🇺🇸 United States

    eWave 6-Lead EKG

    FDA UDI
    Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

    Baby Gorilla/Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795018403·Baby Gorilla, Plate, T2, 10 Hole Locking, 1.1mm...

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012