9151Creatine Kinease
Albania medical device registration · Roche Diagnostics GmbH, Sandhofer Strasse 116, D-68305 Mannheim, Germany · Invitro · Model Creatine Kinease CK 08057460190 · Registered April 02, 2021
- Risk Class
- Invitro
- Product Model
- Creatine Kinease CK 08057460190
- Product Name
- Creatine Kinease
- Registration Date
- April 02, 2021
- Analysis ID
- 9151
Reagent per matjen e kreatine kinazes ne serumin dhe plazmen humane
Access comprehensive regulatory information for Creatine Kinease 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, D-68305 Mannheim, Germany. The device was registered on April 02, 2021.
This page provides complete registration details including product model (Creatine Kinease CK 08057460190), 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.