41 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TENS & PMS (Model: SM9126)
FDA 510(k)
FDA Class 2
·Neurology
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112861·CORNEAL TREPHINE BLADE6.0MM
MILLARD THUMB RETRACTOR HOOK
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896077164·MILLARD THUMB RETRACTOR HOOK SHARP TIPS
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361035978·FENESTRATED SCREW, CANNULATED, Ø10MM x 50MM, SA...
LINK Instruments - Saw and drill guides
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575341412·Orthopaedic implant aiming/guiding block, reusa...
Passeo-14
FDA UDI
Biotronik AG·07640130433861·
Passeo-14
FDA UDI
Biotronik AG·07640130433878·
Passeo-18
FDA UDI
Biotronik AG·07640130430112·
Passeo-14
FDA UDI
Biotronik AG·07640130433885·
DUAL SPIKE TRANSFER DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
CRC-15BT
FDA 510(k)
FDA Class 2
·Radiology
599 SPACE SAVER
FDA Adverse Event
Malfunction
·ALARIS MEDICAL SYSTEMS, INC.·Product code FRN·January 6, 1999
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·August 5, 2020
Spinal needle
FDA UDI
Möller Medical GmbH·04260277172381·
Greene Style needle
FDA UDI
Möller Medical GmbH·04260277172732·
Franseen needle
FDA UDI
Möller Medical GmbH·04260277172565·
Chiba needle
FDA UDI
Möller Medical GmbH·04260277172121·
ONE TOUCH BASIC
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·September 30, 2002
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·February 27, 2002
INTELLIVUE MULTI MEASUREMENT SERVER (MMS)
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 30, 2011