BEUDAMED
    10,000 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 ×

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749000252·CERAMO GRUMME rongeur, 30° angled up, 2.0 x 180 mm

    0412,APS1,08,N,LU,LD

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152334·0412,APS1,08,N,LU,LD

    3601,APS1,08,N,LU,LD

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828151658·3601,APS1,08,N,LU,LD

    GRUMME RONGEUR

    FDA Adverse Event
    Malfunction ·FEHLING INSTRUMENTS GMBH & CO. KG·Product code HTX·February 17, 2017

    3701,APS1,08,N, LU,LD,RA

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828152181·3701,APS1,08,N, LU,LD,RA

    0800,APS1,08,N,LU,LD,IT

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828153232·0800,APS1,08,N,LU,LD,IT

    800,APS1,08,N,LU,LD,IT,BREAKAWAY

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828149433·800,APS1,08,N,LU,LD,IT,BREAKAWAY

    1801,APS0,08,AV,N,LU,LD,RRL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828150026·1801,APS0,08,AV,N,LU,LD,RRL

    FEHLING CE 2MM NLU-2

    FDA Adverse Event
    Malfunction ·FEHLING INSTRUMENTS GMBH & CO. KG·Product code HTX·January 30, 2017

    REPROCESSED BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLU·January 15, 2010

    BIOPSY FORCEPS RADIAL JAW 4 STANDARD CAPACITY W/NEEDLE 2.8MM WORKING CHANNEL

    FDA Adverse Event
    Injury ·STERILMED, INC.·Product code NLU·June 1, 2018

    SOLITAIRE RD

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·March 30, 2025

    SOLITAIRE AB STENT

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NJE·March 30, 2025

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·June 20, 2018

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Death ·ETHICON INC.·Product code GAT·June 20, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 20, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Death ·ETHICON INC.·Product code GAW·June 20, 2018

    REACT CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·March 30, 2025

    Biopsy Forceps, Hot Model #'s: BAL60110 BAR000852 BAR000854 and MIC1550 Laparoscopic electric instruments are designed for use in minimally invasive procedures and open surgical procedures to facilitate coagulation, transection, resection, mobilization, and dissection of tissue.

    FDA Recall
    Terminated ·Sterilmed Inc·Product code NLU·August 8, 2008

    Forceps, Biopsy, Electric, Reprocessed

    FDA classification
    FDA Class 2 ·Forceps, Biopsy, Electric, Reprocessed