44 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Sonishield 100 Antimicrobial Ultrasound Gel
FDA 510(k)
FDA Class 2
·Radiology
AGC TRADITION KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304240858·
BLT Drill, short
FDA UDI
BIO CONCEPT Co., Ltd.·06947600304074·
Oticon
FDA UDI
Oticon A/S·05707131284303·H11V2 TI, BTE 13 WL 85 CNB
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE
Precontoured Rod Ø5.5 mm x70 mm Package
FDA UDI
XENCO MEDICAL LLC·B064XM21510701·
Ø5.5mm X 70mm PRECONTOURED RODS
FDA UDI
XENCO MEDICAL LLC·B064XMPH21510702·
C-QUR RPM MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EXPEDIUM SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TriVerse Femoral Trial
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215098438·
TRILOGY ACETABULAR SYSTEM ECCENTRIC LINER
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code LPH·November 17, 2000
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 6, 2013
CONTRAST INJECTION HIGH PRESSURE TUBING
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DXJ·September 29, 2014
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023