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ACRYLIC POSTERIOR CHAMBER INTRAOCULAR LENS - Argentina Medical Device Registration

Access comprehensive regulatory information for ACRYLIC POSTERIOR CHAMBER INTRAOCULAR LENS in the Argentina medical device market through Pure Global AI's free database. This Registration Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on March 13, 2023.

This page provides complete registration details including product code (1287-86), brand name (VSY), 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 Class III-IV
ACRYLIC POSTERIOR CHAMBER INTRAOCULAR LENS
LENTE INTRAOCULAR ACRILICA DE CAMARA POSTERIOR
Argentina Medical Device Registration
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Product Information

ACRIVA BB UD 613, ACRIVA BB T UDM 611, ACRIVA TRINOVA PRO C, ENOVA GF3.

Device Classification
Registration Type
Registration Class III-IV
Registro Clase III-IV
Product Code
1287-86
Brand Name
VSY
Product Name
ACRYLIC POSTERIOR CHAMBER INTRAOCULAR LENS
LENTE INTRAOCULAR ACRILICA DE CAMARA POSTERIOR
Registration Information
Registration Date
March 13, 2023
Database ID
cmhaytu140a4lekuz2wirm559
Documents
Authorized Representative