Browse medical devices in the “Streptococci” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
261 medical devices in EUDAMED
In vitro diagnostic medical devices › Reagents › Infectious diseases › Bacteriology (infect. immunology/nat)
This is a sub-category of In vitro diagnostic medical devices in the EMDN nomenclature.
Browse all In vitro diagnostic medical devicesVS-GAS172ERisk category
IVDR Class B84354402_MDXRESPB_GAS4VOrganization name
CERTEST BIOTEC S.L.
C3 10343T20-WOERisk category
IVDD — GeneralB-04260743471406Organization name
VELLAP Diagnostics GmbH
R62055Risk category
IVDR Class C50560805PathoDXReagGNOrganization name
Remel Europe Ltd
R30950901Risk category
IVDR Class C50560805StreptexLatexRSOrganization name
Remel Europe Ltd
CFP35P50Risk category
IVDR Class C868511580PCR35JDOrganization name
Vitrosens Biotechnology Inc.
VS-GAS172Risk category
IVDR Class B84354402_MDXRESPB_GAS4VOrganization name
CERTEST BIOTEC S.L.
RD-0059-02 Risk category
IVDD — GeneralB-06971042227639Organization name
SHANGHAI ZJ BIO-TECH CO., LTD
DL239406Risk category
IVDD — GeneralB-06975424223745Organization name
DiYaLab ZJG Biotech Co., Ltd
IP202427-100Risk category
IVDD — GeneralB-08684387212892Organization name
İDİL BİOTECH ARAŞTIRMA SAN. VE TİC. LTD. ŞTİ.
Fa037Risk category
IVDD — GeneralB-697994388Fa037WQ94Organization name
Kangsheng Information Technology (Hangzhou) Co. LTD
PCR35Risk category
IVDD — GeneralB-08685115800213Organization name
Vitrosens Biotechnology Inc.
VS-GAS196TERisk category
IVDR Class B84354402_MDXRESPB_GAS4VOrganization name
CERTEST BIOTEC S.L.
PCR35Risk category
IVDD — GeneralB-08684595033371Organization name
Vitrosens Biotechnology Inc.
R30951001Risk category
IVDR Class C50560805StreptexEnzymeCUOrganization name
Remel Europe Ltd
LYO111Risk category
IVDD — GeneralB-08685115801289Organization name
Vitrosens Biotechnology Inc.
DR0586GRisk category
IVDR Class C5032384StrepGroupLatexPPOrganization name
Oxoid Ltd
R62050Risk category
IVDR Class C50560805PathoDXReagGNOrganization name
Remel Europe Ltd
CGBSZK01A-AHG4ERisk category
IVDD — GeneralB-81649002CGBSZK01A7A8AOrganization name
Healgen Life Science LLC
240938Risk category
IVDR Class B038290MGGIBRZV8GOrganization name
Becton, Dickinson and Company
EBX-039-50Risk category
IVDD — GeneralB-EBX-039-50DMOrganization name
Eurobio Scientific
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 →