Pure Global

Flexible Endoscope (Bronchoscope) - Argentina Medical Device Registration

Access comprehensive regulatory information for Flexible Endoscope (Bronchoscope) 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 February 06, 2024.

This page provides complete registration details including product code (340-121), brand name (Ambu), 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)
Class I-II Registration Modification
Flexible Endoscope (Bronchoscope)
Endoscopio Flexible (broncoscopio)
Argentina Medical Device Registration
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

aScope™ 4 Broncho Slim aScope™ 4 Broncho Regular aScope™ 4 Broncho Large aScope™ 4 Broncho Sampler Set aScope BronchoSampler™ 60 SC

Device Classification
Registration Type
Class I-II Registration Modification
Modificación de Registro Clase I-II
Product Code
340-121
Brand Name
Ambu
Product Name
Flexible Endoscope (Bronchoscope)
Endoscopio Flexible (broncoscopio)
Registration Information
Registration Date
February 06, 2024
Database ID
cmhaytp5r06k2ekuzfgm9lzgt
Authorized Representative