17 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OEC BRIVO 865 ADVANCE, OEC BRIVO 785 ESSENTIAL, AND OEC BRIVO 715 PRIME
FDA 510(k)
FDA Class 2
·Radiology
FOERSTER SPONGE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896021570·FOERSTER SPONGE FORCEPS STRAIGHT SERRATED JAW
Tungsten carbide finisher
FDA UDI
Gebr. Brasseler GmbH & Co. KG·E226100281771·
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011123603000·Carbide bur, coarse
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011123603300·Carbide bur, coarse
Tungsten carbide finisher
FDA UDI
Gebr. Brasseler GmbH & Co. KG·E226100281781·
ZEUS ELISA HSV GG-2 IGG TEST SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
ENDO-GLIDE GUIDEWIRE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 29, 2024
BD SYRINGE 1ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 16, 2025
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·February 7, 2023
ALIGN S URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code OTN·May 17, 2013
CODEMASTER 100
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code LDD·June 10, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
BD SYRINGE 1ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 18, 2024
BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 18, 2021
Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in association with a blood pressure monitor.
FDA Recall
Terminated
·GE Medical Systems Information Technologies·October 24, 2000