Browse medical devices in the “Robotic sample processing systems” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
389 medical devices in EUDAMED
In vitro diagnostic medical devices › Ivd instruments › Sample processing systems
This is a sub-category of In vitro diagnostic medical devices in the EMDN nomenclature.
Browse all In vitro diagnostic medical devices57274Risk category
IVDR Class A805930434ZENITFLOWWYOrganization name
Visia Lab S.r.l.
952054Risk category
IVDR Class A6438153BU0001138FOrganization name
Thermo Fisher Scientific Oy
AS1321Risk category
IVDR Class A08498110517773DOrganization name
Promega Corporation
BB-CVO9603-PS2DRisk category
IVDR Class A697563884BB-CTLDOrganization name
Hangzhou Biobank Bio-technology Co., Ltd.
Innosensia Plus G1ARisk category
IVDR Class A697619397F055LHOrganization name
Shenzhen Shengqiang Technology Co., Ltd.
nizonPLUSRisk category
IVDR Class A805600080nizonPLUSUCOrganization name
HTA s.r.l.
Auflo-G1600Risk category
IVDR Class A697770344GalatekAuflo8AOrganization name
Suzhou MegaRobo Technologies Co.,Ltd
200104000022Risk category
IVDR Class A697615409DX-9000FKOrganization name
Genegeo Diagnostics (Jiangsu) Co., Ltd.
952234Risk category
IVDR Class A6438153BU0001138FOrganization name
Thermo Fisher Scientific Oy
806160Risk category
IVDR Class A76300326806160LXOrganization name
Hamilton Bonaduz AG
67930-03Risk category
IVDR Class A9240106793003XEOrganization name
Seegene, Inc.
P205410101Risk category
IVDR Class A697434507P20PQOrganization name
Amazing Biotech (Shanghai) Co.,LTD
WR086-03-0625Risk category
IVDR Class A805014821IP110ALOOPM03ULOrganization name
Copan Wasp S.r.l.
AS1820Risk category
IVDR Class A08498110646473XOrganization name
Promega Corporation
58022Risk category
IVDR Class A805930434ZENITFLOWCOMP4VOrganization name
Visia Lab S.r.l.
952244Risk category
IVDR Class A6438153BU0001138FOrganization name
Thermo Fisher Scientific Oy
C27703Risk category
IVDR Class A150995904DxAMHOrganization name
Beckman Coulter Biomedical GmbH
Auflo-F1600 ProRisk category
IVDR Class A697770344GalatekAuflo8AOrganization name
Suzhou MegaRobo Technologies Co.,Ltd
Auflo-P1600-S1Risk category
IVDR Class A697770344Auflo6HOrganization name
Suzhou MegaRobo Technologies Co.,Ltd
I7812Risk category
IVDR Class A4987869ICSV40012gCRJOrganization name
Precision System Science 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 →