Browse medical devices in the “Ivd general use consumable devices - other” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
1001 medical devices in EUDAMED
In vitro diagnostic medical devices › Ivd generic use consumables
This is a sub-category of In vitro diagnostic medical devices in the EMDN nomenclature.
Browse all In vitro diagnostic medical devices06970293026251Risk category
IVDR Class A697029302clean001GVOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
10X12”Risk category
IVDR Class A697640013SPB02GSOrganization name
Nanjing Superfit I & E Co., Ltd.
3800209Risk category
IVDR Class A849832003UKOrganization name
Leica Biosystems Richmond, Inc
N.ARisk category
IVDR Class A69552574CT001N8Organization name
Jiangsu Kahotest Citotest Labware Manufacturing Co.,Ltd
06970293023427Risk category
IVDR Class A697029302diluent001DGOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
06970293023281Risk category
IVDR Class A697029302lytic0013NOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
06970293023212Risk category
IVDR Class A697029302clean001GVOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
5830-0009Risk category
IVDR Class A697079159ESRA000A00NQ2Organization name
CITOTEST LABWARE MANUFACTURING CO.,LTD
FR2MPRisk category
IVDR Class A85942104700000000FREUOrganization name
LabMediaServis s.r.o.
06970293020563Risk category
IVDR Class A697029302clean001GVOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
C31Risk category
IVDR Class A697092794CULTURE0016ZOrganization name
Zhejiang Aicor Medical Technology Co., Ltd.
VCMAR-W1Risk category
IVDR Class A843604032VCMAR-W101QXOrganization name
Vircell, S.L
06970293026169Risk category
IVDR Class A697029302clean001GVOrganization name
Zhejiang xinke Medical Technology Co., Ltd.
N/ARisk category
IVDR Class A697095264POCTA001EPOrganization name
Jiangsu Kehua Medical Instrument Technology Co., Ltd.
4004-0803Risk category
IVDR Class A697079159ASCA000A00N9DOrganization name
CITOTEST LABWARE MANUFACTURING CO.,LTD
3800201AERisk category
IVDR Class A849832003UKOrganization name
Leica Biosystems Richmond, Inc
H-105Risk category
IVDR Class A698036138HDFOrganization name
Shandong Chengwu Ronghua Biotechnology Co., Ltd.
Blue/Yellow/White Pipette Tip For Gilson（Filter）1000ul/200ul/10ulRisk category
IVDR Class A697734624PT01QJOrganization name
YIWU EASON MEDICAL DEVICES CO.,LTD.
16mlRisk category
IVDR Class A697826803KWCTUZOrganization name
Taizhou Kangwei Medical Instrument Co., Ltd.
500mlRisk category
IVDR Class A697937794WAB01WNOrganization name
HAIMEN SHENGBANG LABORATORY EQUIPMENT 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 →