25 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
UNIDUS MALE LATEX CONDOM (WITH COLOR AND FLAVORING)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668114056·J-SHAPED CANNULA 25GA ANGLED (PK/10)
DRX - Ascend System
FDA UDI
CARESTREAM HEALTH, INC.·60889971023179·DRX-ASCEND SYSTEM/QG-40-3-R10-T140
COMPUMEDICS SIESTA SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
TM2000 EASYTRACE PLUS RECEIVING CENTER
FDA 510(k)
FDA Class 2
·Cardiovascular
True Position®
FDA UDI
ATLAS SPINE, INC.·M68112080231750·31mm x 7.5mm Non-Lordotic Spacer
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011
audifon
FDA UDI
audifon GmbH & Co. KG·EADF023175904733217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0231759047312017201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF023175904731317201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0231759047338217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0231759047338117201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF023175904731217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0231759047312717201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF023175904732517201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF0231759047315917201·RITE-TRT
OSCILLATING SAW ATTACH
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL S.A.·Product code GFA·February 27, 2013
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 15, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 4, 2008