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Airship Guide - Argentina Medical Device Registration

Access comprehensive regulatory information for Airship Guide in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on August 14, 2024.

This page provides complete registration details including product code (651-466), brand name (Back-up Meier), 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 modification (non-agile) Class III-IV
Airship Guide
Guรญa Dirigible
Argentina Medical Device Registration
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Product Information

H965SCH306010 0,035'' 300 cm Ex, Flexible C Tip H965SCH306011 0,035'' 300 cm Ex, Flexible C Tip B/5 H965SCH306000 0,035'' 185 cm, Flexible J Tip H965SCH306001 0,035'' 185 cm, Flexible J Tip B/5 M001306021 0,035'' 260 cm, C Tip B/5

Device Classification
Registration Type
Registration modification (non-agile) Class III-IV
Modificaciรณn de Registro (no รกgil) Clase III-IV
Product Code
651-466
Brand Name
Back-up Meier
Product Name
Airship Guide
Guรญa Dirigible
Registration Information
Registration Date
August 14, 2024
Database ID
cmhayu5bd0kdbekuzoqwl52kx
Authorized Representative