43 results
·
22ms
·
Sources: EU EUDAMED, US FDA
SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM
FDA 510(k)
FDA Class 2
·Radiology
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950016655·CURETTE MOLT 2/4 7" 18CM
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964002425·Custom Procedure Kit
Affiniti
FDA UDI
TORNIER, INC.·00846832024445·HUMERAL HEAD TRIAL
Zimmer
FDA UDI
Preat Corporation·00842092129326·Zimmer® TSV-compatible 5.5mm X 3.0mm Healing Ab...
SR Facebow
FDA UDI
ORMCO CORPORATION·00889989023206·Facebow SHORT SZ 1 .044 DIA.
OsteoMed
FDA UDI
OSTEOMED LLC·00845694026857·PrimaLOK SP Retractor Extension
QB1 NMES System
FDA UDI
Motive Health, Inc.·00854691008308·QB1 NMES System; XS, Right
e-vive NMES System; Extra Small, Right (2.0 Dock)
FDA UDI
Motive Health, Inc.·00854691008469·e-vive NMES System; Extra Small, Right (2.0 Dock)
FOGARTY ARTERIAL CATHETER
FDA Adverse Event
EDWARDS DIV. BAXTER HEALTHCARE CORP.·Product code DXE·December 23, 1993
AESCULAP BONE WAX
FDA 510(k)
FDA Unclassified
·Unknown
IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB
FDA 510(k)
FDA Class 2
·Immunology
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 8, 2021