32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964001565·Custom Procedure Kit
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741042706·Catheter Placement Kit
TruFlex
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730011916·Truflex™ PT SE NiTi Upper 19x25 38mm 10/PK
TruFlex™
FDA UDI
Ortho Organizers, Inc.·00190707127367·Truflex™ PT SE NiTi Upper 19x25 38mm (10PK)
Spex Limited
FDA UDI
SPEX LIMITED·09420051771499·Constructa Ischial Insert. Suits Flex or Shape ...
Patient Cable
FDA UDI
GLOBAL INSTRUMENTATION, LLC·90815187020078·Patient Cable 3L IEC
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167900001420·
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014601076·E-Z Lift Beach Chair - Mizuho
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167S1900001420·
GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ELECSYS B-CROSSLAPS CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014601069·E-Z Lift Beach Chair (EU) - Mizuho
Alteon
FDA UDI
Exactech, Inc.·10885862555601·ALT CUP TRL G1 SIZE 42
CARDIOSAVE HYBRID W/ E/F PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·January 5, 2026
SEDI-40 INSTR.
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·September 13, 2022
SPECTRA OPTIA
FDA Adverse Event
TERUMO BCT·Product code LKN·March 12, 2013
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·February 18, 2011
ACCU-CHEK AVIVA
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code NBW·February 19, 2008
BD SEDI-40 INSTR. DEFECTIVE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·February 3, 2022