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ANVISA registration 80102519052Active

SILICONE GEL IN TUBE

ANVISA Registration Number: 80102519052VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDASTRATPHARMA AGRisk Class I
Verified
Device names
Technical name
SILICONE GEL IN TUBE
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PT: GEL DE SILICONE EM BISNAGA
Commercial name
Strataderm
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Risk class
Class I
Registration details
Registration Number
80102519052
Process Number
25351042926201709
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
STRATPHARMA AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Feb 20, 2017
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for SILICONE GEL IN TUBE in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80102519052 and manufactured by STRATPHARMA AG. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.