BEUDAMED
    874 results · 38ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ENDO TECH INSTRUMENTS

    FDA registration
    ENDO TECH INSTRUMENTS·61 products·🇵🇰 Pakistan

    isolate

    FDA UDI
    Endo/Tech·D052I5NLMB1·isolate Non Latex Dental Dam in Medium Blue. E...

    ENDO-TECH LTD., TIPS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FIEGERT ENDOTECH CYSTOSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MW5079152

    FDA Adverse Event
    Malfunction ·August 14, 2018

    ENDO STITCH 10MM

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code OCW·March 1, 2019

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code OCW·April 23, 2021

    1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", sterile; 4. UNIMAX Detachable endo pocket, REF FEP936116, 3" x 6", sterile; 5. UNIMAX Detachable endo pocket, REF FEP979000, 8" x 10", sterile; 6. ConMed Corporation Detachable endo pocket, REF SB936, 3" x 6", sterile; 7. ConMed Corporation Detachable endo pocket, REF SB957, 5" x 7", sterile; 8. ConMed Corporation Detachable endo pocket, REF SB979, 7.5" x 9", sterile; 9. ConMed Corporation Detachable endo pocket, REF SB979-CA, 7.5 x 9", sterile; 10. ConMed Corporation Detachable endo pocket, REF SB936-CA, 3" x 6", sterile;

    FDA Enforcement
    Class II ·Ongoing·UNIMAX MEDICAL SYSTEMS INC·September 25, 2024

    SENSATION SHORT THROW

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code FDI·January 4, 2019

    ENDO GIA ULTRA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GAG·February 12, 2014

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDW·July 25, 2014

    SURGIDAC

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GAR·October 25, 2016

    SURGIDAC

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code OCW·March 14, 2017

    ENDO STITCH* SURGIDAC*2/0 48 GRN DLU TU

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·October 20, 2016

    ICC

    FDA Adverse Event
    ERBE USA, INC·Product code GEI·October 16, 2014

    VLOCK 180 RELOAD

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GAM·February 25, 2025

    ENDO GIA STAPLER LOAD

    FDA Adverse Event
    Malfunction ·COVIDIEN (UNITED STATES SURGICAL CORP)·Product code GDW·September 29, 2008

    MULTI FIRE ENDO GIA 30

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·July 2, 1998

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL, A DIVISION OF TYCO HEALTHCARE·Product code KOG·November 11, 2013