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Thrombectomy Instrument - Argentina Medical Device Registration

Access comprehensive regulatory information for Thrombectomy Instrument in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on April 12, 2024.

This page provides complete registration details including product code (310-109), brand name (PHENOX), 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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Revalidation of Registration I-II-III-IV
Thrombectomy Instrument
Instrumento para Trombectomรญa
Argentina Medical Device Registration
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Product Information

PRE-4-20 PRE-6-30 PRESS-5-40 PRES 6-50 PRE-LT 3-20 PRE-LT 4-20 PRE-LUX-4-20

Spanish:

PRE-4-20 PRE-6-30 PRES-5-40 PRES 6-50 PRE-LT 3-20 PRE-LT 4-20 PRE-LUX-4-20

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
310-109
Brand Name
PHENOX
Product Name
Thrombectomy Instrument
Instrumento para Trombectomรญa
Registration Information
Registration Date
April 12, 2024
Database ID
cmhaytks50227ekuzcnzoilyv
Authorized Representative