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Albania AKBPM registration 9224

Atellica IM SARS-CoV-2 IgG, Atellica IM SARS-CoV-2 IgG Quality Control

AlbaniaSiemens Healthcare Diagnostics Inc. 511 Benedict Avenue, Tarrytown, NY, 10591-5097, USAInvitroModel Atellica IM SARS-CoV-2 IgG – 11206997 (1-pack) Atellica IM SARS-CoV-2 IgG – 11206998 (5-pack) Atellica IM SARS-CoV-2 IgG Quality Control - 11206999Registered April 19, 2021
VerifiedAKBPM · official registry
Device classification
Risk Class
Invitro
Product Model
Atellica IM SARS-CoV-2 IgG – 11206997 (1-pack) Atellica IM SARS-CoV-2 IgG – 11206998 (5-pack) Atellica IM SARS-CoV-2 IgG Quality Control - 11206999
Product Name
Atellica IM SARS-CoV-2 IgG, Atellica IM SARS-CoV-2 IgG Quality Control
Registration information
Registration Date
April 19, 2021
Analysis ID
9224
Manufacturer
Name
Siemens Healthcare Diagnostics Inc. 511 Benedict Avenue, Tarrytown, NY, 10591-5097, USA
Product information

Reagent per identifikimin e Sars-CoV-2

About this record

Access comprehensive regulatory information for Atellica IM SARS-CoV-2 IgG, Atellica IM SARS-CoV-2 IgG 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 IgG – 11206997 (1-pack) Atellica IM SARS-CoV-2 IgG – 11206998 (5-pack) Atellica IM SARS-CoV-2 IgG Quality Control - 11206999), 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.