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Atellica IM Sars-CoV-2 Total; Atellica IM Sars-CoV-2 Total Quality Control - Albania Medical Device Registration

Access comprehensive regulatory information for Atellica IM Sars-CoV-2 Total; Atellica IM Sars-CoV-2 Total Quality Control 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 April 19, 2021.

This page provides complete registration details including product model (Atellica IM Sars-CoV-2 Total 11206711 (1-pack); Atellica IM Sars-CoV-2 Total 11206923 (5-pack); Atellica IM Sars-CoV-2 Total Quality Control 11206712), 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
Atellica IM Sars-CoV-2 Total; Atellica IM Sars-CoV-2 Total Quality Control
Albania Medical Device Registration
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Product Information

Teste per diagnostikimin e Sars-Cov-2 dhe kontrolle te cilesise

Device Classification
Risk Class
Invitro
Product Model
Atellica IM Sars-CoV-2 Total 11206711 (1-pack); Atellica IM Sars-CoV-2 Total 11206923 (5-pack); Atellica IM Sars-CoV-2 Total Quality Control 11206712
Product Name
Atellica IM Sars-CoV-2 Total; Atellica IM Sars-CoV-2 Total Quality Control
Registration Information
Registration Date
April 19, 2021
Analysis ID
9223