12 results
·
68ms
·
Sources: EU EUDAMED, US FDA
RESTON SELF ADHERING FOAM
FDA Adverse Event
Injury
·3M MEDICAL PRODUCTS GROUP·Product code KGX·April 28, 1997
ADULT BOVIE PAD
FDA Adverse Event
Malfunction
·3M MEDICAL PRODUCTS GROUP·Product code GEI·January 17, 1997
ARTHROSCOPY PUMP
FDA Adverse Event
Other
·MEDICAL PRODUCTS GROUP, 3M CO.·Product code HRX·July 19, 1996
KITTMANN DEFIBRILLATOR PAD
FDA Adverse Event
Injury
·MEDICAL PRODUCTS GROUP 3M CO.·Product code LDD·June 21, 1996
VITREBOND
FDA Adverse Event
Injury
·3M·Product code EMA·February 22, 2017
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 30, 2024
Jiangxi 3L Medical Products Group Co., Ltd.
Manufacturer
🇨🇳 China·TÜV Rheinland LGA Products GmbH
DZ 2048293-1
Certificate
MDR QA·Jiangxi 3L Medical Products Group Co., Ltd.·TÜV Rheinland LGA Products GmbH
phoenix Medtech GmbH
Authorized representative
🇩🇪 Germany·66 Manufacturers·1059 Devices
Shanghai International Holding Corp. GmbH(Europe)
Authorized representative
🇩🇪 Germany·637 Manufacturers·33064 Devices
RIOMAVIX LTD
Authorized representative
🇪🇸 Spain·400 Manufacturers·4531 Devices
Wellkang Ltd
Authorized representative
259 Manufacturers·3500 Devices