10,000 results
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43ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TALENT
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 10, 2013
HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic use by laboratory professionals in clinical laboratories. The assay provides quantitative results on 3.2% citrated human plasma Part Number: 0020302602
FDA Recall
Open, Classified
·Instrumentation Laboratory·Product code QLU·August 25, 2021
Anti-Factor Xa Activity Test System, Apixaban
FDA classification
FDA Class 2
·Anti-Factor Xa Activity Test System, Apixaban
BLU-LAB LLC
FDA registration
BLU-LAB LLC·2 products·🇺🇸 United States
PLU OPHTHALMIC Corp
FDA registration
PLU OPHTHALMIC Corp·1 product·🇺🇸 United States
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929079·BLU LASER GOGGLES SINGLE
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929161·BLU LASER BASE CHARGER
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919928980·BLU LASER TIPS 5MM 25PK
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919928959·BLU LASER STARTER KIT
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929048·BLU LASER BATTERY LITHION
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929130·BLU LASER POWER SUPPLY
Blu
FDA UDI
TRIDENT SRL·08055060430405·Digital intra oral sensor for radiographic exam...
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929109·BLU LASER CARBON FILM
BLU
FDA UDI
Peter Brasseler Holdings, LLC·00887919929017·BLU LASER TIPS 7MM 25PK
BEIJING HUAN QIU LI KANG BIOTECH CO., LTD.
FDA registration
BEIJING HUAN QIU LI KANG BIOTECH CO., LTD.·1 product·🇨🇳 China
MICROLUX/BLU
FDA 510(k)
FDA Class 1
·Dental
ALU-KART
FDA 510(k)BLUING REAGENT
FDA 510(k)
FDA Class 1
·Pathology
CORE 500 Digital Stethoscope - Sapphire Bundle
FDA UDI
Eko Devices, Inc.·00850010298641·CORE 500 Digital Stethoscope - Sapphire Bundle
Plum QuickFix
FDA UDI
Plum Safety ApS·05715205900011·Plum QuickFix plasters are intended as first ai...