BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    ORIA SPINAL SYSTEM, DOMINO AND TUBE CONNECTORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Graves Vu-More X Long 7" (178mm)

    FDA UDI
    MEDGYN PRODUCTS, INC.·M803030958·Graves Vu-More X Long 7" (178mm)

    INTENSIV SA

    FDA registration
    INTENSIV SA·4 products·🇨🇭 Switzerland

    ATAC PAK BUN REAGENT AND ATAC CALIBRATOR KITS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    COALESCENT U-CLIP DELIVERY AND DISPOSAL DEVICE

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2013

    COOK GUNTHER TULIP

    FDA Adverse Event
    Injury ·COOK·Product code DTK·March 23, 2011

    OVATIO

    FDA Adverse Event
    Malfunction ·ELA MEDICAL·Product code LWS·April 16, 2008

    FREESTYLE GLUCOMETER AND STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT·Product code LFR·February 8, 2018

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018