10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MRSA/SA ELITE MGB, ELITE MGB SOFTWARE
FDA 510(k)
FDA Class 2
·Microbiology
K152468
FDA UDI
Shenzhen Vistar Medical Supplies Co.,Ltd.·96973521874184·Reusable NIBP cuff,Thigh,single tube, HP connector
Oticon
FDA UDI
Oticon A/S·05707131257741·H15, BTE 13 WL 100 SIL
SUTURTEK FASTCLOSE STERNUM CLOSURE DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ZOLL PROPAQ MD
FDA 510(k)
FDA Class 2
·Cardiovascular
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
HARMONIC ACE 36CM W ERG HANDLE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 22, 2008
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·June 17, 2011
UNKNOWN DRILL
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HAW·June 9, 2025
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026