133 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700 SERIES) LEVELS, 1,2 AND 3, MODEL 507, 508, 509
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TOPCUT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
THERMO DMA FRUCTOSAMINE ASSAY, MODEL 7500-135/235
FDA 510(k)
FDA Class 2
·Hematology
Reicodent
FDA UDI
devemed GmbH·04061644035090·Periodontal Probe # CP15 "N. Carolina"
graduate...
Reicodent
FDA UDI
devemed GmbH·04061644035120·Periodontal Probe # CP11
graduated; 3-6-8-11 mm...
Reicodent
FDA UDI
devemed GmbH·04061644039623·TITAN-Periodontal Probe # CP15"North Ca"
gradua...
Reicodent
FDA UDI
devemed GmbH·04061644035113·Periodontal Probe # CP11.5B (WHO)
graduated; 3,...
Reicodent
FDA UDI
devemed GmbH·04061644037568·Periodontal Probe # Gold.-Fox | Williams
gradua...
Reicodent
FDA UDI
devemed GmbH·04061644026142·Furcation probe "Nabers" # CQ-2N
graduated; 3-6...
Reicodent
FDA UDI
devemed GmbH·04061644035083·Periodontal Probe # EX3A/CP15
graduated; 1-2......
Reicodent
FDA UDI
devemed GmbH·04061644035106·Periodontal Probe # CP12
graduated; 3-6-9-12 mm...
Reicodent
FDA UDI
devemed GmbH·04061644035137·Periodontal Probe # CP2
graduated; 2-4-6-8-10-1...
Reicodent
FDA UDI
devemed GmbH·04061644062799·Periodontal Probe # 23/CP15
graduated; 1-2...-1...
Reicodent
FDA UDI
devemed GmbH·04061644035076·Periodontal Probe # 23/CP12
graduated; 3-6-9-12...
CYSTOTOME CYSTOENTEROSTOMY NEEDLE KNIFE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code KNS·March 15, 2019
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·March 21, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·February 15, 2011
STERIS SYSTEM 1
FDA Adverse Event
Other
·STERIS CORPORATION·Product code MLR·March 24, 2008
ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·April 8, 2026
ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·April 1, 2026