Albania AKBPM registration 9151

Creatine Kinease

Name: Creatine Kinease — Albania device registration 9151
Creator: Roche Diagnostics GmbH, Sandhofer Strasse 116, D-68305 Mannheim, Germany
Keywords: Creatine Kinease, Creatine Kinease CK 08057460190, Roche Diagnostics GmbH, Sandhofer Strasse 116, D-68305 Mannheim, Germany, Invitro, Albania medical device

AlbaniaRoche Diagnostics GmbH, Sandhofer Strasse 116, D-68305 Mannheim, GermanyInvitroModel Creatine Kinease CK 08057460190Registered April 02, 2021

VerifiedAKBPM · official registry

Device classification

Risk Class: Invitro
Product Model: Creatine Kinease CK 08057460190
Product Name: Creatine Kinease

Registration information

Registration Date: April 02, 2021
Analysis ID: 9151

Manufacturer

Name: Roche Diagnostics GmbH, Sandhofer Strasse 116, D-68305 Mannheim, Germany

Product information

Reagent per matjen e kreatine kinazes ne serumin dhe plazmen humane

About this record

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.