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Nelaton catheters - Argentina Medical Device Registration

Access comprehensive regulatory information for Nelaton catheters in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration 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 (414-175), brand name (MFLAB, Flexguard, Foyomed.), 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
Nelaton catheters
Catรฉteres de Nelaton
Argentina Medical Device Registration
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Product Information

8Fr, 10Fr, 12Fr, 14Fr, 16Fr, 18Fr 20Fr, 22Fr.

Device Classification
Registration Type
Class I-II Registration
Registro Clase I-II
Product Code
414-175
Brand Name
MFLAB, Flexguard, Foyomed.
Product Name
Nelaton catheters
Catรฉteres de Nelaton
Registration Information
Registration Date
July 30, 2024
Database ID
cmhayu5bf0kidekuzhvtdut0j
Authorized Representative