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SINGLE-USE PERICRANIAL NEEDLES - Argentina Medical Device Registration

Access comprehensive regulatory information for SINGLE-USE PERICRANIAL NEEDLES in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Modification medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on April 26, 2024.

This page provides complete registration details including product code (1440-78), brand name (DC, HONGDA, SQL, MCM, EUROMIX), 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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Class I-II Registration Modification
SINGLE-USE PERICRANIAL NEEDLES
AGUJAS PERICRANEALES DE USO UNICO
Argentina Medical Device Registration
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Product Information

27G, 26G, 25G, 24G, 23G, 22G, 21G, 20G, 19G, 18G, 16G.

Device Classification
Registration Type
Class I-II Registration Modification
Modificaciรณn de Registro Clase I-II
Product Code
1440-78
Brand Name
DC, HONGDA, SQL, MCM, EUROMIX
Product Name
SINGLE-USE PERICRANIAL NEEDLES
AGUJAS PERICRANEALES DE USO UNICO
Registration Information
Registration Date
April 26, 2024
Database ID
cmhaytks401zlekuznbo9pq0j
Authorized Representative