29 results
·
22ms
·
Sources: EU EUDAMED, US FDA
VARIAN HIGH ENERGY LINEAR ACCELERATOR
FDA 510(k)
FDA Class 2
·Radiology
SCHWARTZ VESSEL CLIP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008900·SCHWARTZ VESSEL CLIP STRAIGHT
Ear Coupler Set
FDA UDI
PATH medical GmbH·04260223145315·Ear Coupler Set (5 pcs.)
NITANIUM® ARCHWIRES
FDA UDI
Ortho Organizers, Inc.·00190707065782·.019 X .025 Upper Coated Nitanium® Pro Form™ Ar...
Ear Coupler Set
FDA UDI
PATH medical GmbH·04260223143427·Ear Coupler Set (25 pcs.)
Portex
FDA UDI
ICU MEDICAL, INC.·15019315060397·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315060380·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315107184·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315107160·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315060403·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315107177·
CHAD THERAPEUTICS OXYMATIC MODEL 401
FDA 510(k)
FDA Class 2
·Anesthesiology
BD ULTRA-FINE II INSULIN SYRINGE-MINI NEEDLE, MODEL 30G * 3/16 (5MM)
FDA 510(k)
FDA Class 2
·General Hospital
HAHN TAPERED IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 7, 2025
HAHN TAPERED IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 11, 2025
HAHN TAPERED IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 17, 2025
UNKNOWN IMPLANT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·March 23, 2010
OPTETRAK LOGIC
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 27, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·September 12, 2014