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Reagente - Albania Medical Device Registration

Access comprehensive regulatory information for Reagente in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Siemens Healthcare Diagnostics Inc. 511 Benedict Avenue, Tarrytown, NY, 10591-5097, USA. The device was registered on February 03, 2022.

This page provides complete registration details including product model (CLINITEK Atlasโ„ข Control Strips ; CLINTEK Atlasโ„ข Reagents; CLINITEK Novusโ„ข Reagents (sipas listes bashkalidhur) ), 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
Reagente
Albania Medical Device Registration
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Product Information

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Device Classification
Risk Class
Invitro
Product Model
CLINITEK Atlasโ„ข Control Strips ; CLINTEK Atlasโ„ข Reagents; CLINITEK Novusโ„ข Reagents (sipas listes bashkalidhur)
Product Name
Reagente
Registration Information
Registration Date
February 03, 2022
Analysis ID
8809