628 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ONLINE TDM Vancomycin Gen.3
FDA 510(k)
FDA Class 2
·Clinical Toxicology
1.5 LACTOSORB SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036054960·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741522450·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674152245060·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970478·
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161121522450·Bridgeback Acetabular Reamer, Size 45mm
ACCENT AND EXCEED SERIES ORTHODONTIC CERAMIC BRACKETS
FDA 510(k)
FDA Class 2
·Dental
CARE ZY5BA OXYGEN CONCENTRATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
Exactech, Inc.·10885862282743·TRIAL, MONOBLOC REVISION STEM, 15x245mm
N/A
FDA UDI
Exactech, Inc.·10885862659781·Trial, Monobloc Revision Stem
REVO MRI SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWP·June 7, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 23, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 10, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 13, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 22, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 31, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 10, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 20, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·July 27, 2021