Pure Global AI
ANVISA registration 81086830107Active

AUTOTESTE PARA VITAMINA D

ANVISA Registration Number: 81086830107FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDAVEDALABRisk Class II
Verified
Device names
Technical name
AUTOTESTE PARA VITAMINA D
View exact technical-name matches →
Commercial name
Vitamin D-Screen
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
81086830107
Process Number
25351166607202569
CNPJ
20037992000139
Company information
Registration Holder
FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA
Manufacturer
VEDALAB
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Nov 03, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for AUTOTESTE PARA VITAMINA D in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81086830107 and manufactured by VEDALAB. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS 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.