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cobas e 402 analytical unit. - Argentina Medical Device Registration

Access comprehensive regulatory information for cobas e 402 analytical unit. in the Argentina medical device market through Pure Global AI's free database. This IVD Modification Group A and B medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 01, 2024.

This page provides complete registration details including product code (740-783), brand name (cobas e 402 analytical unit.), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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IVD Modification Group A and B
cobas e 402 analytical unit.
Argentina Medical Device Registration
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Product Information

Cat Nยฐ 09031553001: cobas e 402 analytical unit.

Device Classification
Registration Type
IVD Modification Group A and B
Modificaciรณn IVD Grupo A y B
Product Code
740-783
Brand Name
cobas e 402 analytical unit.
Product Name
cobas e 402 analytical unit.
Registration Information
Registration Date
July 01, 2024
Database ID
cmhayu5bh0kp4ekuz5he4ua0v
Authorized Representative
Name
ROCHE S.A. PRODUCTS
PRODUCTOS ROCHE S.A.