28 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KARMAN WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
PERMITE
FDA UDI
SDI LIMITED·09336472000387·PERMITE 2SP FAST 50
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040062517·Endoflex Reamers 21 mm
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950018567·FORCEP MOSQUITO #3 HALSTED CURVED 4-3/4" 12CM
SoftTip® small
FDA UDI
Honeywell Healthcare Solutions GmbH·04036616009928·SoftTip® small RS-3211-31 MySign® FDA
PERMITE
FDA UDI
SDI LIMITED·DO3640022022·
SCANLAN®
FDA UDI
SCANLAN INTERNATIONAL INC·00846159018370·Vascular Clamp with straight Hausmann Jaw
4.0 X 22mm CANN SCREW FASTENER Ti LG THD
FDA UDI
Osteocentric Technologies, Inc.·00810074303446·4.0 X 22mm CANN SCREW FASTENER Ti LG THD
CORTEK LAPAROSCOPES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SUREFIT DISPERSIVE ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEYER-SCHULTE MAMMARY PROSTHESIS
FDA Adverse Event
MENTOR CORP.·Product code FWM·May 24, 1994
BD PLASTIPAK LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·January 9, 2021
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 13, 2013
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 12, 2014
PROPEX
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·February 4, 2011
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 23, 2019
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 23, 2019
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 23, 2019
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 23, 2019
UNKNOWN BIO-INTRAFIX
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·July 23, 2019