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Albania AKBPM registration 9444

Elecsys β- CrossLaps/serum - 07026960190

AlbaniaRoche Diagnostics GmbH, Sandhofer Strasse 116,D- 68305 Mannheim, GermanyInvitroModel Elecsys β- CrossLaps/serum - 07026960190Registered May 25, 2021
VerifiedAKBPM · official registry
Device classification
Risk Class
Invitro
Product Model
Elecsys β- CrossLaps/serum - 07026960190
Product Name
Elecsys β- CrossLaps/serum - 07026960190
Registration information
Registration Date
May 25, 2021
Analysis ID
9444
Manufacturer
Name
Roche Diagnostics GmbH, Sandhofer Strasse 116,D- 68305 Mannheim, Germany
Product information

Reagent per matjen e β- CrossLaps ne serumin dhe plazmen humane .

About this record

Access comprehensive regulatory information for Elecsys β- CrossLaps/serum - 07026960190 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 May 25, 2021.

This page provides complete registration details including product model (Elecsys β- CrossLaps/serum - 07026960190), 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.