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Dual lumen catheter and access kit - Argentina Medical Device Registration

Access comprehensive regulatory information for Dual lumen catheter and access kit 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 01, 2024.

This page provides complete registration details including product code (251-120), brand name (MC3), 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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Registration Class III-IV
Dual lumen catheter and access kit
Catéter dual lumen y kit de acceso
Argentina Medical Device Registration
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Product Information

70413 Crescent RA Catéter dual lumen 13 FR 70415 Crescent RA Catéter dual lumen 15 FR 70419 Crescent RA Catéter dual lumen 19 FR 71824 Crescent RA Catéter dual lumen 24 FR 70124 Crescent Yugular Catéter dual lumen 24 FR 70126 Crescent Yugular Catéter dual lumen 26 FR 70128 Crescent Yugular Catéter dual lumen 28 FR 70130 Crescent Yugular Catéter dual lumen 30 FR 70132 Crescent Yugular Catéter dual lumen 32 FR 21030 Opus Kit de acceso vascular

Device Classification
Registration Type
Registration Class III-IV
Registro Clase III-IV
Product Code
251-120
Brand Name
MC3
Product Name
Dual lumen catheter and access kit
Catéter dual lumen y kit de acceso
Registration Information
Registration Date
March 01, 2024
Database ID
cmhayu4ft0jjsekuzkh3s0ec6
Documents
Authorized Representative