Atellica IM Sars-CoV-2 Total; Atellica IM Sars-CoV-2 Total Quality Control

Albania medical device registration · Siemens Healthcare Diagnostics Inc. 511 Benedict Avenue, Tarrytown, NY, 10591-5097, USA · Invitro · 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 · Registered April 19, 2021

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

Manufacturer

Name: Siemens Healthcare Diagnostics Inc. 511 Benedict Avenue, Tarrytown, NY, 10591-5097, USA

Product information

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

About this record

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.