28 results
·
23ms
·
Sources: EU EUDAMED, US FDA
CLEARVIEW EXACT II INFLUENZA A & B TEST
FDA 510(k)
FDA Class 2
·Microbiology
AGXO
FDA UDI
Oticon A/S·05707131164803·K140, BTE 13 CBE AGXO
Carbide burs
FDA UDI
DFS - DIAMON GmbH·04057176153630·Carbide 25R FG 1,0 mm
PAL400 Pressure feeler 400g
FDA UDI
SEDATELEC·03760262492926·The Palpeur is a device for pressure applying. ...
M2A 38MM
FDA UDI
Biomet Uk Ltd·05019279908684·
General Instrument
FDA UDI
ALPHATEC SPINE, INC.·00840180510940·Long Pedicle Markers - no inserter
LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PERIFIX SAFETY EPIDURAL NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
T-PLUS™* PEEK VBR/IBF SYSTEM
FDA UDI
Pioneer Surgical Technology, Inc.·00846468032692·T-Plus, 10X36X10
T-Plus PEEK IBF System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468088538·INTERBODY FUSION DEVICE
T-Plus PEEK IBF System
FDA UDI
Pioneer Surgical Technology, Inc.·00846468088613·INTERBODY FUSION DEVICE
T-PLUS™* PEEK VBR/IBF SYSTEM
FDA UDI
Pioneer Surgical Technology, Inc.·00846468032708·T-Plus, 10X36X10, 6 DEG LORDOTIC
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code LOX·December 16, 2022
TREK¿
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LOX·May 27, 2025
PROGRASP (TM) FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 9, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 19, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 26, 2011
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246786637·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246786545·
Fortilink Cages with TiPlus Technology
FDA UDI
Baat Medical Products B.V.·08720246786705·