Pure Global

Guidewire Extension Catheter - Argentina Medical Device Registration

Access comprehensive regulatory information for Guidewire Extension Catheter in the Argentina medical device market through Pure Global AI's free database. This 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 March 22, 2024.

This page provides complete registration details including product code (877-203), brand name (Nipro), 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.

Free Database
Powered by Pure Global AI
Argentina ANMAT Data
Bilingual (Spanish/English)
Registration Class III-IV
Guidewire Extension Catheter
Catรฉter de Extensiรณn de Guรญa
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

GUIDEPLUS II ST GUIDEPLUS II EL

Device Classification
Registration Type
Registration Class III-IV
Registro Clase III-IV
Product Code
877-203
Brand Name
Nipro
Product Name
Guidewire Extension Catheter
Catรฉter de Extensiรณn de Guรญa
Registration Information
Registration Date
March 22, 2024
Database ID
cmhaytn4s044dekuzou4xp5el
Documents
Authorized Representative