Browse medical devices in the “Blood grouping instruments” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
102 medical devices in EUDAMED
In vitro diagnostic medical devices › Ivd instruments › Hematology / histology / cytology instruments
This is a sub-category of In vitro diagnostic medical devices in the EMDN nomenclature.
Browse all In vitro diagnostic medical devices0066056Risk category
IVDR Class A40420910001U3KOrganization name
IMMUCOR Medizinische Diagnostik GmbH
Aigel 50Risk category
IVDR Class A697462121AigelV9Organization name
Aikang MedTech Co., Ltd
Metis Pro 200-8sRisk category
IVDR Class A697462121Metis3FOrganization name
Aikang MedTech Co., Ltd
0089000Risk category
IVDR Class A88823401W0202030185A000UQOrganization name
Immucor, Inc.
Aigel 980Risk category
IVDR Class A697462121AG9809MOrganization name
Aikang MedTech Co., Ltd
GT2013Risk category
IVDR Class A93543300GT20138TOrganization name
Haemokinesis Ltd
0066055Risk category
IVDR Class A88823405W0202030185A51MBOrganization name
IMMUCOR Medizinische Diagnostik GmbH
Metis Pro 150-6QRisk category
IVDR Class A697462121Metis3FOrganization name
Aikang MedTech Co., Ltd
GT2015Risk category
IVDD — GeneralB-09354330000577Organization name
Haemokinesis Ltd
Aigel 980ARisk category
IVDR Class A697462121AG9809MOrganization name
Aikang MedTech Co., Ltd
N555BLRisk category
Class I081259401N55100M9Organization name
Neotech Products LLC
Metis Pro 150-8Risk category
IVDR Class A697462121Metis3FOrganization name
Aikang MedTech Co., Ltd
MS036800Risk category
IVDR Class A150995901MS036800CSOrganization name
Beckman Coulter Inc.
210700Risk category
IVDR Class A843658373DGREADERNET77Organization name
Diagnostic Grifols, S.A.
TDB515Risk category
IVDR Class A697388160109NPOrganization name
Tianjin Dexiang Biotechnology Co., Ltd.
Metis Pro 210-8sRisk category
IVDR Class A697462121Metis3FOrganization name
Aikang MedTech Co., Ltd
Aigel 90-4sRisk category
IVDR Class A697462121AigelV9Organization name
Aikang MedTech Co., Ltd
0066056Risk category
IVDR Class A88823405W0202030185A50M9Organization name
IMMUCOR Medizinische Diagnostik GmbH
VNEORisk category
Class IB-00195893005314Organization name
Translite, LLC
808-502-35Risk category
Class I896110278OTOVIS8086AOrganization name
Medical Devices (Pvt) 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 →