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Sterile Disposable Scalpel Blade - Argentina Medical Device Registration

Access comprehensive regulatory information for Sterile Disposable Scalpel Blade in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Revalidation medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 16, 2023.

This page provides complete registration details including product code (420-22), brand name (Rib), 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 Revalidation
Sterile Disposable Scalpel Blade
Hoja de bisturí desechable estéril
Argentina Medical Device Registration
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Product Information

Sterile Scalpel Blades for Small Handle: Handle 3, Blade Size 9 to 17 Large Handle Sterile Scalpel Blades: Handle 4, Blade Size 18 to 36T

Spanish:

Hojas de bisturí estéril para mango pequeño: mango 3, tamaño de hoja 9 a 17 Hojas de bisturí estéril para mango grande: mango 4, tamaño de hoja 18 a 36D

Device Classification
Registration Type
Class I-II Registration Revalidation
Reválida de Registro Clase I-II
Product Code
420-22
Brand Name
Rib
Ribbel
Product Name
Sterile Disposable Scalpel Blade
Hoja de bisturí desechable estéril
Registration Information
Registration Date
June 16, 2023
Database ID
cmhayu4fy0jz3ekuzkb0r1vkw
Authorized Representative