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Safetouch Pericranial Needle Equipment - Argentina Medical Device Registration

Access comprehensive regulatory information for Safetouch Pericranial Needle Equipment in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on June 17, 2024.

This page provides complete registration details including product code (877-90), 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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Revalidation of Registration I-II-III-IV
Safetouch Pericranial Needle Equipment
Equipo de Agujas Pericraneales Safetouch
Argentina Medical Device Registration
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Product Information

Safetouch 18G x ¾" (19mm), Safetouch 19G x ¾" (19mm), Safetouch 20G x ¾" (19mm), Safetouch 21G x ¾" (19mm), Safetouch 22G x ¾" (19mm), Safetouch 23G x ¾" (19mm), Safetouch 24G x ¾" (19mm), Safetouch 25G x ¾" (19mm), Safetouch 26G x ¾" (19mm), Safetouch 27G x ¾" (19mm).

Spanish:

Safetouch 18G x ¾” (19mm), Safetouch 19G x ¾” (19mm), Safetouch 20G x ¾” (19mm), Safetouch 21G x ¾” (19mm), Safetouch 22G x ¾” (19mm), Safetouch 23G x ¾” (19mm), Safetouch 24G x ¾” (19mm), Safetouch 25G x ¾” (19mm), Safetouch 26G x ¾” (19mm), Safetouch 27G x ¾” (19mm).

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
877-90
Brand Name
Nipro
Product Name
Safetouch Pericranial Needle Equipment
Equipo de Agujas Pericraneales Safetouch
Registration Information
Registration Date
June 17, 2024
Database ID
cmhayu5bi0ks6ekuzixu19i9k
Authorized Representative