BEUDAMED
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    FDA UDI
    Synthes GmbH·00845384017493·Otologic Curved Micro (OCM) Attachment

    Anspach

    FDA UDI
    Synthes GmbH·00845384017721·Otologic Curved Micro (OCM) Attachment, G1

    OCM-G1 Attachment

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OCR II & OCM II

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OXYGEN CONSUMPTION MONITOR #OCM-0100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511074203·NYLON CUFF W/2-TUBE BLADDER-OCM-BULK

    MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 11, 2026

    NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·February 11, 2026

    OXYCODONE 20 NG/ML

    FDA UDI
    UTAK LABORATORIES, INC.·B800OXY20WBOCME0·OXYCODONE 20 NG/ML

    TRACHEAL INTUBATION FIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·October 19, 2016

    HF UNIT "ESG-400"

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 6, 2016

    OCM STERILIZER

    FDA Adverse Event
    Malfunction ·PELTON & CRANE, A DCI CO.·Product code FLE·November 11, 1999

    EVIS LUCERA BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·June 13, 2018

    AMS 800 URINARY CONTROL SYSTEM WITH INHIBIZONE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·November 30, 2018

    DRUGS OF ABUSE 3

    FDA UDI
    UTAK LABORATORIES, INC.·B800DAWB3V2OCME0·DRUGS OF ABUSE 3

    DRUGS OF ABUSE 3

    FDA UDI
    UTAK LABORATORIES, INC.·B800DAWB3V3OCME0·DRUGS OF ABUSE 3

    HD AUTOCLAVABLE CAMERA HEAD

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·May 22, 2017

    OVATION

    FDA Adverse Event
    Injury ·ORTHO DEVELOPMENT·Product code LPH·July 22, 2020

    PURITAN BENNETT

    FDA Adverse Event
    Malfunction ·NELLCOR-PURITAN BENNETT·Product code CBK·October 30, 2003