Browse medical devices in the “Immunoglobulin e - total” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
210 medical devices in EUDAMED
In vitro diagnostic medical devices › Reagents › Immunochemistry (immunology) › Allergy
This is a sub-category of In vitro diagnostic medical devices in the EMDN nomenclature.
Browse all In vitro diagnostic medical devices36090000Risk category
IVDD — GeneralB-04260153751310Organization name
Gold Standard Diagnostics Kassel GmbH
1N1100 98Risk category
IVDR Class A8058945151N110098ZVOrganization name
ABD SRL
DL245506Risk category
IVDD — GeneralB-06975424223998Organization name
DiYaLab ZJG Biotech Co., Ltd
MD1107050Risk category
IVDD — GeneralB-08431673940102Organization name
Spinreact S.A.U.
200 Tests/kit（DR1139-3）Risk category
IVDD — GeneralB-06974969982902Organization name
Biobase Diagnostic Technology (Shandong) Co., Ltd.
W107ARisk category
IVDD — GeneralB-06971824209075Organization name
Shenzhen Tisenc Medical Devices Co., Ltd.
93WRisk category
IVDD — GeneralB-26974969791546Organization name
Chongqing iSIA BIO-Technology Co., Ltd.
IEDGX-B00/AURisk category
IVDD — GeneralB-05415168006606Organization name
Diagam S.A.
IEDGX-B00Risk category
IVDD — GeneralB-05415168006552Organization name
Diagam S.A.
JL1107050Risk category
IVDD — GeneralB-08431673088422Organization name
Spinreact S.A.U.
016Risk category
IVDD — GeneralB-06976043630167Organization name
iCarbonX IntelliCore (Guangdong) Co., Ltd.
50-01Risk category
IVDD — GeneralB-04251557100019Organization name
Astra Biotech GmbH
32027218Risk category
IVDD — GeneralB-06950334822950Organization name
Genrui Biotech Inc.
GGIGE-302aRisk category
IVDD — GeneralB-GGIGE-302aX2Organization name
Zhejiang Orient Gene Biotech Co., Ltd
50-01ARisk category
IVDD — GeneralB-04251557100026Organization name
Astra Biotech GmbH
50-03Risk category
IVDD — GeneralB-04251557109036Organization name
Astra Biotech GmbH
7-231Risk category
IVDD — GeneralB-05907514672318Organization name
PZ CORMAY Spółka Akcyjna
CFPC-91Risk category
IVDR Class C880613300117BROrganization name
Boditech Med Inc.
TK1107050Risk category
IVDD — GeneralB-08431673370503Organization name
Spinreact S.A.U.
0320511601Risk category
IVDD — GeneralB-06975984067421Organization name
Shenzhen Lifotronic Technology Co., Ltd.
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →