Browse medical devices in the “Gastro-intestinal lavage tubes and sets” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
326 medical devices in EUDAMED
Gastrointestinal devices › Gastrointestinal tubes and sets
This is a sub-category of Gastrointestinal devices in the EMDN nomenclature.
Browse all Gastrointestinal devices4105.2.10070Risk category
Class I40375662000LZOrganization name
Albert Hohlkörper GmbH & Co. KG
6900510Risk category
Class I733338724104D3Organization name
Wellspect HealthCare
20686Risk category
Class I42502032PRI0024COrganization name
Primed Halberstadt Medizintechnik GmbH
6930930Risk category
Class I733338724104D3Organization name
Wellspect HealthCare
20676Risk category
Class I42502032PRI0024COrganization name
Primed Halberstadt Medizintechnik GmbH
9232Risk category
Class IIa89040459230TEOrganization name
Vitromed Healthcare
EN ISO 20695:2020Risk category
Class IIa697594680JSCZWTstomach6BOrganization name
Changzhou Weite Medical Equipment Co.,Ltd.
WG-Fr14Risk category
Class IIa69267672003XDOrganization name
Shandong Steve Medical Science & Technology Co., Ltd.
6901381Risk category
Class I733338724104D3Organization name
Wellspect HealthCare
70113Risk category
Class I426031921000colon6HOrganization name
Hänsler Medical GmbH
GC1908Z32L13C01Risk category
Class I697450061SU0212003N79Organization name
GCMEDICA ENTERPRISE LTD.(WUXI)
20697Risk category
Class I42502032PRI0024COrganization name
Primed Halberstadt Medizintechnik GmbH
6901712Risk category
Class I733338724104D3Organization name
Wellspect HealthCare
6900710Risk category
Class I733338724104D3Organization name
Wellspect HealthCare
EN ISO 20695:2020Risk category
Class IIa697594680JSCZWTstomach6BOrganization name
Changzhou Weite Medical Equipment Co.,Ltd.
PIC 20 009Risk category
Class I40375662000LZOrganization name
Albert Hohlkörper GmbH & Co. KG
6FrRisk category
Class IIaB-06948097057009Organization name
Haiyan Kangyuan Medical Instrument Co.,Ltd.
20699Risk category
Class I42502032PRI0024COrganization name
Primed Halberstadt Medizintechnik GmbH
40486Risk category
Class I890209540480FBOrganization name
Poly Medicure Limited
EN ISO 20695:2020Risk category
Class IIa697594680JSCZWTstomach6BOrganization name
Changzhou Weite Medical 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 →