26 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283761·HOOK SKIN RIGID 1 PRONG BLUNT 6.5"
Simpact Tri-Fin
FDA UDI
Life Spine, Inc.·00190837063030·Parallel Pin Offset Guide, Large Screw
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776370992·Rigid Neck Rake Retractor
Trial Liners (Neutral and 10 degree hooded)
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215038502·
MAGNETOM SYSTEMS WITH SOFTWARE SYNGO MR 2006A
FDA 510(k)
FDA Class 2
·Radiology
HEMOSIL PROTEIN S ACTIVITY ASSAY
FDA 510(k)
FDA Class 2
·Hematology
BD VERITOR¿ RAPID DETECTION OF SARS-COV-2
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·October 5, 2021
URETEX SUP URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·May 24, 2013
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Malfunction
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 24, 2011
MYNX
FDA Adverse Event
Malfunction
·ACCESS CLOSURE INC·Product code MGB·August 15, 2008
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 25, 2024
ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX
FDA Enforcement
Class III
·Terminated·Ameditech Inc·December 30, 2015
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024