9 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FORA TD-3224 BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Tiger Supply Inc.
FDA UDI
TIGER SUPPLY, INC.·D82360817141·VPS Impression Material Medium Body Regular Set...
Stamey
FDA UDI
COOK INCORPORATED·00827002148116·Stamey Percutaneous Loop Suprapubic Catheter Set
MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149
FDA 510(k)
FDA Class 2
·Anesthesiology
BIPAP PRO BI-LEVEL SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JUMAO MEDICAL EQUIPMENT·Product code IOR·April 29, 2013
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·July 25, 2008
MYNX VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·ACCESSCLOSURE, INC.·Product code MGB·May 9, 2011
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V
FDA Enforcement
Class II
·Terminated·Roche Diagnostics Corporation·March 14, 2018