41 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CEROX, MODEL 321OF
FDA 510(k)
FDA Class 2
·Cardiovascular
Bur PM2-70 80K steel Ø3.5x80 sterile
FDA UDI
Bien-Air Surgery SA·17630055513042·
Micro Clamp Applier Forceps
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896118195·Micro Clamp Applier Forceps
TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896082250·TISSUE FORCEPS TUNGSTEN CARBIDE SERRATED TIP
MICRO CLIP APPLIER FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008750·MICRO CLIP APPLIER FORCEPS
MICRO CLIP APPLIER FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003804·MICRO CLIP APPLIER FORCEPS
Tiche PTA Balloon Dilatation Catheter
FDA UDI
BrosMed Medical Co.,Ltd.·06958481476705·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315059414·
Monoblock Tibial Trial UC Insert
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215043605·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047374·
Zavation
FDA UDI
Zavation LLC·00197157002244·7.5mm Cannulated Tap
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047350·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047336·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047435·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047411·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315047398·
HYCARE LATEX EXAMINATION GLOVE, POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
ASSAYED QCS 1,2, CAT. NOS. 970200, 970500
FDA 510(k)
FDA Class 1
·Clinical Chemistry
20ML LUER LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·June 19, 2020
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024