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ANVISA registration 80102513488Valid until Jul 28, 2035

Cannulas

ANVISA Registration Number: 80102513488VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDADORNIER MEDTECH AMERICARisk Class III
Verified
Device names
Technical name
Cannulas
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PT: Cânulas
Commercial name
Dornier SmartFlex - Cânula de Fibra Laser Reutilizável
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Risk class
Class III
Registration details
Registration Number
80102513488
Process Number
25351083349202586
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
DORNIER MEDTECH AMERICA
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Jul 28, 2025
Validity
28/07/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Cannulas in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513488 and manufactured by DORNIER MEDTECH AMERICA. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jul 28, 2035.

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.