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CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD - Albania Medical Device Registration

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.

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Invitro
CKMB 05168562190 UDI-DI 7613336000069H; CKMB 08057486190 UDI-DI 761333600516AD
Albania Medical Device Registration
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Product Information

Reagent per analizen e CKMB te serumit ne plazmen humane.

Device Classification
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 Information
Registration Date
July 30, 2021
Analysis ID
9964