BEUDAMED
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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749042139·Andrews Pynchon Suction 3.0 x 240 mm

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749042146·Andrews Pynchon Suction 4.2 x 240 mm

    Lace Bite Pad - S/M- No Logo

    FDA UDI
    Silipos Holding LLC·00614464319051·

    SIGMA SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 10, 2025

    HTG CASING

    FDA Adverse Event
    Malfunction ·G.E. MEDICAL SYSTEMS·Product code ITY·March 25, 2004

    BEAR 1000

    FDA Adverse Event
    ALLIED HEALTHCARE PRODUCTS, INC.·Product code CBK·January 23, 1997

    VITEK® 2 GRAM-POSITIVE SUSCEPTIBILITY TEST KIT AST-P605

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, INC.·Product code LON·February 4, 2016

    HUDSON AQUAPAK WITH ADAPTOR

    FDA Adverse Event
    Malfunction ·TELEFELX MEDICAL·Product code BTT·July 7, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·October 11, 2013

    NEBULIZER ADAPTOR

    FDA Adverse Event
    Malfunction ·TELEFELX MEDICAL·Product code CAF·May 3, 2010

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 28, 2025

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·March 12, 2018

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·August 6, 2018

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·September 7, 2012

    CAPIOX FX15 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTZ·June 2, 2015

    HUDSON NON-REBREATHING MASK W/O SAFETY VENT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BYG·March 13, 2013

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·April 19, 2023

    ARCTIC SUN DEVICE

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·November 15, 2023

    G90 BUILT IN S/M NO XFRMR-P&C

    FDA Adverse Event
    Malfunction ·DENTSPLY LLC·Product code ELC·September 4, 2019

    ACCU-CHEK ® AVIVA EXPERT

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code NBW·April 20, 2018