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Albania AKBPM registration 11598

In vitro medical devices

AlbaniaRoche Diagnostics GmbH, Sandhofer Strasse 116, 68305 Mannheim, GermanyInvitroModel In Vitro Medical Devices: ETHO2 5967104190 (UDI-DI 761333600783B6); ETOH2 03183777190 (UDI-DI 761333600586B2); ETOH2 08057630190 (UDI-DI 761333600640AF); ETOH2 08445672190 (UDI-DI 761333600688BB);Registered March 25, 2022
VerifiedAKBPM · official registry
Device classification
Risk Class
Invitro
Product Model
In Vitro Medical Devices: ETHO2 5967104190 (UDI-DI 761333600783B6); ETOH2 03183777190 (UDI-DI 761333600586B2); ETOH2 08057630190 (UDI-DI 761333600640AF); ETOH2 08445672190 (UDI-DI 761333600688BB);
Product Name
In vitro medical devices
Registration information
Registration Date
March 25, 2022
Analysis ID
11598
Manufacturer
Product information

Reagent per matjen e etanolit ne gjakun human

About this record

Access comprehensive regulatory information for In vitro medical devices in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Roche Diagnostics GmbH, Sandhofer Strasse 116, 68305 Mannheim, Germany. The device was registered on March 25, 2022.

This page provides complete registration details including product model (In Vitro Medical Devices: ETHO2 5967104190 (UDI-DI 761333600783B6); ETOH2 03183777190 (UDI-DI 761333600586B2); ETOH2 08057630190 (UDI-DI 761333600640AF); ETOH2 08445672190 (UDI-DI 761333600688BB);), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.