31 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE MICROKERATOME BLADES-PE
FDA 510(k)
FDA Class 1
·Ophthalmic
Leksell Stereotactic System
FDA UDI
Elekta Instrument AB·07340048305280·ARC AXIS RING COUNTER SCALE
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001176·artVeneer life upper anteriors, BIM, B1
5 piece ClipRay Biodegradable PSP/FILM Size 0/1/2 Holder
FDA UDI
CLIKTECH LLC·00856200001176·5 piece ClipRay Biodegradable PSP/FILM Size 0/1...
5.7Ah Li-ion Battery
FDA UDI
PHYSIO-CONTROL, INC.·00885074765730·BATTERY PACK-LI-ION, E-CELL
KerraMax Care Gentle Border
FDA UDI
CRAWFORD HEALTHCARE LIMITED·05060077234208·
PEACE OF MIND MULTIPLE DRUGS OF ABUSE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MASTERSITE NEEDLELESS LUER ACTIVATED IV CONNECTOR, MODEL MS 1000
FDA 510(k)
FDA Class 2
·General Hospital
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
9616240-2006-00339
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00340
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
SILASTIC HIGH TEC TRIPLE WALL LOW BLEED BREAST IMPLANT
FDA Adverse Event
Injury
·MCGHAN MEDICAL CORP.·Product code FTR·May 19, 1994
9616240-2006-00350
FDA Adverse Event
Malfunction
·Product code FII·June 23, 2006
9616240-2006-00345
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 4, 2024
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013