Browse medical devices in the “Mycoplasma / ureaplasma” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
299 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 devicesKZ-402-12Risk category
IVDD — GeneralB-38594036044020Organization name
VIDIA spol. s r.o.
81033Risk category
IVDR Class C803389132CHORUSMYA00B6Organization name
DIESSE Diagnostica Senese S.p.A
ID024Risk category
IVDD — GeneralB-06974323012979Organization name
Beijing Applied Biological Technologies Co., Ltd.
JB(Z)60104NW-24TRisk category
IVDD — GeneralB-JB(Z)60104NW-24T5FOrganization name
Jiangsu Bioperfectus Technologies Co., Ltd.
86-03-24Risk category
IVDD — GeneralB-04251557109289Organization name
Astra Biotech GmbH
IM4415040Risk category
IVDR Class B69506174IM441040D7Organization name
Maccura Biotechnology Co., Ltd.
ODZ-010Risk category
IVDD — GeneralB-28594036040100Organization name
VIDIA spol. s r.o.
VS-MGR113LERisk category
IVDR Class B84354402_MDXRESIST_MGRMZOrganization name
CERTEST BIOTEC S.L.
MG/MC/190Risk category
IVDD — GeneralB-08595696301989Organization name
GeneProof a.s.
IM4407041Risk category
IVDD — GeneralB-IM4407041JFOrganization name
Maccura Biotechnology Co., Ltd.
LMP0120Risk category
IVDD — GeneralB-06974566302189Organization name
Zhuhai Encode Medical Engineering Co., Ltd.
86-01-56Risk category
IVDD — GeneralB-04251557109241Organization name
Astra Biotech GmbH
STI1-RT50Risk category
IVDD — GeneralB-TRMF000028405STI1RT50J4Organization name
GENMARK SAĞLIK ÜRÜNLERİ İTHALAT İHRACAT VE TİCARET LİMİTED ŞİRKETİ
GCMP(IgM)-302aRisk category
IVDD — GeneralB-GCMP(IgM)-302aHGWROrganization name
Healgen Scientific Limited Liability Company
C2KC004Risk category
IVDD — GeneralB-06976753477625Organization name
Hangzhou Cybereagen Biotech Co., Ltd.
MYCG0350DSRisk category
IVDD — GeneralB-+ENTIMYCG0350DS00Organization name
Gold Standard Diagnostics Frankfurt GmbH
C2KJ015Risk category
IVDD — GeneralB-06971792053533Organization name
Hangzhou Realy Tech Co.,Ltd.
ID041Risk category
IVDD — GeneralB-06974323010876Organization name
Beijing Applied Biological Technologies Co., Ltd.
ITSZ092001Risk category
IVDD — GeneralB-06974912093747Organization name
Nexlab Co., Ltd.
C88003G-LRisk category
IVDR Class C692591270093HJOrganization name
SHENZHEN YHLO BIOTECH 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 →