BEUDAMED
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    SOVEREIGN BIPOLAR INSTRUMENTS

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

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF.CON.

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·August 21, 2015

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00133001·

    Silicone hose 6x2,5 2m

    FDA UDI
    Drägerwerk AG & Co. KGaA·04048675414605·

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001330·artVeneer life upper anteriors, CL, C2

    Rampart One Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7401001330·Trial 18mm M 16°

    Midmark IQecg® Digital ECG

    FDA UDI
    MIDMARK CORPORATION·00841709100581·The IQecg® from Midmark is an easy-to-use, digi...

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NITRILE PATIENT EXAMINATION GLOVE (GREEN COLOR), POWDER FREE, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TEMA ELBOW

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JDC·November 18, 2022

    IMPAX CV 7.8SU3

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·March 13, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 24, 2011

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 19, 2008

    Xhibit Telemetry Receiver, Model: 96280

    FDA Enforcement
    Class II ·Ongoing·Spacelabs Healthcare, Inc.·August 17, 2022