25 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STEAMPLUS STERILIZATION TEST
FDA 510(k)
FDA Class 2
·General Hospital
APC™ PLUS Unitek™ Mini Uni-Twin
FDA UDI
3M UNITEK CORPORATION·00652221092663·Mini Uni-Twin(TM) Bracket APC(TM) PLUS Standard...
APC™ II Unitek™ Mini Uni-Twin
FDA UDI
3M UNITEK CORPORATION·00652221061645·Mini Uni-Twin(TM) Bracket APC(TM) II Standard E...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756397858·General Purpose Temperature Probe
3M™ Unitek™ Uni-Twin™
FDA UDI
3M UNITEK CORPORATION·00652221015730·Mini Uni-Twin(TM) Bracket Standard Edgewise UL3...
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756927499·General Purpose Temperature Probe
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036020606·
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756046145·General Purpose Temperature Probe
MAXONE, BLOOD, BLOOD PRODUCTS AND IV FLUID WARMER
FDA 510(k)
FDA Class 2
·General Hospital
MODIFICATION TO T-REX BIOPSY FORCEPS
FDA 510(k)
FDA Class 2
·Cardiovascular
CERENOVUS ENTERPRISE
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code NJE·September 15, 2025
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·December 30, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 1, 2014
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 1, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 15, 2013
81-020409 GENERAL PURPOSE PROBE YSI400
FDA Adverse Event
Other
·DEROYAL INDUSTRIES, INC.·Product code FLL·April 4, 2003
81-020409 GENERAL PURPOSE PROBE YSI400
FDA Adverse Event
Malfunction
·DEROYAL SINDUSTRIES, INC.·Product code FLL·December 2, 2002
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·February 8, 2011
PHILIPS
FDA Adverse Event
PHILIPS MEDICAL SYSTEMS·Product code LNH·March 13, 2008