BEUDAMED
    24 results · 22ms · 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 ×

    1.5 M PROPANEDIOL FREEZING MEDIUM, 1.5 PROPANEDIOL 0.1 SUCROSE FREEZING MEDIUM, 9% GLYCEROL, 0.2 M SUCROSE FREEZING MEDI

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

    1801 P37,GE,BE,2L,2LD,BE (7&8),STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828101073·1801 P37,GE,BE,2L,2LD,BE (7&8),STKR

    HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2

    FDA 510(k)
    FDA Class 2 ·Dental

    ANTI-BLASTOMYCES SERUM #CF10027X

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

    MAMMOTOME HARDWARE HOLSTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

    MAMMOTOME CONTROL MODULES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KNW·June 13, 2006

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·March 6, 2013

    DEXATIP

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·February 15, 2011

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 8, 2014

    TI LOCK-SCR CANCLS 6.5X35MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 13, 2018

    TI LOW PROFILE SCREW 6.5X45MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 13, 2018

    TI LOCK-SCR CANCLS 6.5X30MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 13, 2018

    TI LOW PROFILE SCREW 6.5X35MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 13, 2018

    TI LOW PROFILE SCREW 6.5X40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 13, 2018

    TI LOCK-SCR CANCLS 6.5X40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 13, 2018