333 results
·
21ms
·
Sources: EU EUDAMED, US FDA
TI-1000 TRANSPORT INCUBATOR
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252599678·CUSTOMIZED MAND. RECON PLATE28, FULL
ihcDirect® PTH Ab, 5mL
FDA UDI
NOVODIAX, INC.·00850000596764·Clone C123
ihcDirect® PTH Ab, 15mL
FDA UDI
NOVODIAX, INC.·00850000596771·Clone C123
ihcDirect® PTH Ab Conjugate 15mL
FDA UDI
NOVODIAX, INC.·00850030934581·Clone C123
ihcDirect® PTH Ab Conjugate 5mL
FDA UDI
NOVODIAX, INC.·00850030934574·Clone C123
THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
FDA 510(k)
FDA Class 2
·Dental
PENTAX VIDEO BRONCHOSCOPES (EB FAMILY)
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
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
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·May 23, 2014
SUREFIRE SCORPION NEEDLE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MDM·November 14, 2012
ATLAS PLUS DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010