9964CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD
Albania medical device registration · Roche Diagnostic GmbH Sandhofer Strasse 116 68305 Mannheim Germany · Invitro · Model CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD · Registered July 30, 2021
- Risk Class
- Invitro
- Product Model
- CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD
- Product Name
- CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD
- Registration Date
- July 30, 2021
- Analysis ID
- 9964
Reagent per analizen e CKMB te serumit ne plazmen humane.
Access comprehensive regulatory information for CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Roche Diagnostic GmbH Sandhofer Strasse 116 68305 Mannheim Germany. The device was registered on July 30, 2021.
This page provides complete registration details including product model (CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD), 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.