28 results · 21ms · Sources: EU EUDAMED, US FDA

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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