BEUDAMED
    18 results · 18ms · Sources: EU EUDAMED, US FDA

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    BIOSTATOR PRINTER/PLOTTER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RTI Allograft Paste

    FDA UDI
    Rti Surgical, Inc.·00898623002026·Allograft Paste 10cc

    Health Care Logistics, Inc®

    FDA UDI
    Health Care Logistics, Inc.·10827989000350·Adapter Cap 20mm/B

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209120758·KIT, MERET TFAK PRO X w' CGLE - BLK

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515207677·Swiss Blade Breaker and Holder

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450179338·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930780121030·Bayonet Bipolar Forcep 1.0mm 8" working

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197494304·Micro Scissors curved...

    NIPRO SAFETOUCH HUBER INFUSTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HI-RES 9000 PHASED ARRAY CAROTID COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROFILE 8 FR. 40 CC. IAB WITH ACCESSORIES-DOMESTIC

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·October 10, 1998

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 8, 2014

    ECHELON*FLEX60 LONG

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 23, 2012

    ARTICUL/EZE BALL 28 +1.5 GR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·August 11, 2010

    Paraffin Pretreatment Reagent Kit II; each kit contains the following: 5 x 50 mL Pretreatment Solution (sodium thiocyanate - NaSCN), 5 x 62.5 mL Protease Buffer II (0.2N HCl), 5 x 250 mg Protease I (Pepsin, lyophilized, activity 1:3000 to 1:3500); Abbott Molecular Inc; list 07J02-002, part number 32-801210. invitro diagnostic.

    FDA Recall
    Terminated ·Abbott Molecular·Product code KEO·January 22, 2010

    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

    paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·October 2, 2024

    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·March 27, 2024