25 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ROCHE DIAGNOSTICS CK-MB
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TruForm
FDA UDI
Rmo, Inc.·00885797099709·MX MLR BDS R/L SE ASIA ASST100
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828117494·GEN4 INTERACTIVE
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159008586·Micro Forceps, Round Handle, str DD platform ti...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450482872·
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159018936·TITANIUM MICRO FORCEPS ROUND HANDLE STRT PLTFM ...
SCANLAN® Titanium Neuro Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159012002·Micro Suture Tying Fcp, RH, Gerald type taper, ...
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159008593·Micro Forceps, Round Handle, str DD platform ti...
SCANLAN® Titanium Neuro Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159036268·Micro Suture Tying Fcp, RH, Gerald type taper, ...
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159008609·Micro Forceps, Round Handle, str DD platform ti...
SCANLAN® Titanium Forceps
FDA UDI
SCANLAN INTERNATIONAL INC·00846159008616·Micro Forceps, Round Handle, str DD platform ti...
INSET GUARD
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·March 30, 2026
VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EBI XFIX DFS METAPHYSEAL CORRECTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ALLOFT-S ALLOCLASSIC SHL 52/II
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code JDI·March 12, 2019
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
CLARION
FDA Adverse Event
Malfunction
·ADVANCED BIONICS, LLC·Product code MCM·February 14, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 12, 2014
ALLOFIT-S ALLOCLASSIC, SHELL WITH POLAR SCREW PLUG, UNCEMENTED, 52/II
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 27, 2018
INFUSOMAT®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·November 15, 2023