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Infusion set - Argentina Medical Device Registration

Access comprehensive regulatory information for Infusion set 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 July 08, 2024.

This page provides complete registration details including product code (877-132), 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.

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Argentina ANMAT Data
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Class I-II Registration Modification
Infusion set
Set de infusión
Argentina Medical Device Registration
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Product Information

Sets de infusión (estéril, de un solo uso): IS-150/AV/L/PI-WB, IS-150/NV/S/PI-WB, IS-170/AV/RL/PI-WB, IS-170/NV/RL/PI-WB, IS-170/AVF/RL/H-WB, IS-17M/AVF/RL/H-WB, IS-170P/AV/RL-WB, IS-170PFH/AV/RL-WB, IS-185P/AV/RL-WB, IS-185PFH/AV/RL-WB, IS-200P/AV/RL-WB, IS-200PFH/AV/RL-WB, IS-200BBC/AV/RL-WB, IS-200BBS/AV/RL-WB Set de infusión con bureta: MG-100SV-WB, MG-150SV-WB, MG-100CV-WB, MG-150CV-WB, MG-100CV-WB/, MG-150CV-WB/, MG-100CV/NFP-WB, MG-150CV/NFP-WB, MG-100CV/NFAH-WB, MG-150CV/NFAH-WB

Device Classification
Registration Type
Class I-II Registration Modification
Modificación de Registro Clase I-II
Product Code
877-132
Brand Name
Nipro
Product Name
Infusion set
Set de infusión
Registration Information
Registration Date
July 08, 2024
Database ID
cmhaytq4a0768ekuzakatjix9
Authorized Representative