4,842 results
·
43ms
·
Sources: EU EUDAMED, US FDA
MTIC_017-2019
Certificate
MDD Annex II Section 4·IDS LTD.·MTIC InterCert S.r.l.·1 Basic UDI-DI
0068/QCO-DM/055-2018
Certificate
MDD Annex II Section 4·IDS LTD.·MTIC InterCert S.r.l.·3 Basic UDI-DIs
Rf Identification
FDA classification
FDA Not Classified
·Rf Identification
Antigen, Id, Candida Albicans
FDA classification
FDA Class 2
·Antigen, Id, Candida Albicans
Human Leukocyte Antigen (Hla) Typing Companion Diagnostic Test
FDA classification
FDA Class 2
·Human Leukocyte Antigen (Hla) Typing Companion Diagnostic Test
ALPHAMED LTD
Importer
3 Manufacturers
Candida Spp., Direct Antigen, Id
FDA classification
FDA Class 2
·Candida Spp., Direct Antigen, Id
Determine HIV Early Detect
Basic UDI-DI
EU IVDD
·
Eu Ivd Annex 2 List A
·Abbott Diagnostics Medical Co., Ltd.·1 device
EDTA Capillary Tubes
Basic UDI-DI
EU IVDR
·
Eu Ivd Class A
·Abbott Diagnostics Medical Co., Ltd.·1 device
Determine HIV Controls
Basic UDI-DI
EU IVDD
·
Eu Ivd Annex 2 List A
·Abbott Diagnostics Medical Co., Ltd.·1 device
Chase Buffer
Basic UDI-DI
EU IVDR
·
Eu Ivd Class A
·Abbott Diagnostics Medical Co., Ltd.·1 device
Reprocessed Bronchoscope
FDA classification
FDA Class 2
·Reprocessed Bronchoscope
Implantable Radio Frequency Transponder System
FDA classification
FDA Class 2
·Implantable Radio Frequency Transponder System
Antigen, Cf And / Or Id, Coccidioides Immitis
FDA classification
FDA Class 2
·Antigen, Cf And / Or Id, Coccidioides Immitis
Synthon auto-injector (brand names:MyJect, Autoxon, Perscleran, Sensigo)
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Synthon Hispania S.L.·2 devices
V7 103108 0005
Certificate
IVDD Annex IV Section 4·Abbott Diagnostics Medical Co., Ltd.·TÜV SÜD Product Service GmbH·1 Basic UDI-DI
V7 103108 0007
Certificate
IVDD Annex IV Section 4·Abbott Diagnostics Medical Co., Ltd.·TÜV SÜD Product Service GmbH·1 Basic UDI-DI
Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
FDA classification
FDA Class 2
·Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
AKRALAB S.L.U.
Importer
🇪🇸 Spain·8 Manufacturers
System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
FDA classification
FDA Class 2
·System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection