22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNDUS MALE LATEX CONDOM (WITH FLAVORING)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668114063·MCINTYRE-BINKHORST CAN 25GA ANG RT PK/10
NA
FDA UDI
STERILMED, INC.·10888551019842·SAW BLADE MICRO OSCILLATING CRESCENTIC 32MM CUT...
NA
FDA UDI
STERILMED, INC.·10888551017831·SAW BLADE MICRO OSCILLATING CRESCENTIC 32MM CUT...
CONMED
FDA UDI
Conmed Corporation·10845854002254·MICRO OSCILLATOR BLADE, CRESCENTIC, 13.5 X 32 X...
BIOEMG II AND BIOJVA
FDA 510(k)
FDA Class 2
·Physical Medicine
MODIFICATION TO: SENS-A-RAY SYSTEM WITH PROIMAGE SOFTWARE
FDA 510(k)
FDA Class 2
·Dental
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
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
AIR DERMATOME HANDPIECE
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL·Product code GFD·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