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Pulmonary artery monitoring catheter - Argentina Medical Device Registration

Access comprehensive regulatory information for Pulmonary artery monitoring catheter in the Argentina medical device market through Pure Global AI's free database. This Modification of Agile Registration Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on July 30, 2024.

This page provides complete registration details including product code (2315-83), brand name (BIOPTIMAL), 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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Argentina ANMAT Data
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Modification of Agile Registration Class III-IV
Pulmonary artery monitoring catheter
Catรฉter de monitorizaciรณn de la arteria pulmonar
Argentina Medical Device Registration
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Product Information

TD2602NX 110cm 6C

Spanish:

TD2602NX 110cm 6F

Device Classification
Registration Type
Modification of Agile Registration Class III-IV
Modificaciรณn de Registro รgil Clase III-IV
Product Code
2315-83
Brand Name
BIOPTIMAL
Product Name
Pulmonary artery monitoring catheter
Catรฉter de monitorizaciรณn de la arteria pulmonar
Registration Information
Registration Date
July 30, 2024
Database ID
cmhayu5bf0khkekuz1li43xzb
Authorized Representative