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ANVISA registration 81733730024Active

HEMOGLOBIN SUBTYPE

ANVISA Registration Number: 81733730024TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDATRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDARisk Class III
Verified
Device names
Technical name
HEMOGLOBIN SUBTYPE
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PT: HEMOGLOBINA SUBTIPO
Commercial name
PREMIER RESOLUTION REAGENT KIT
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Risk class
Class III
Registration details
Registration Number
81733730024
Process Number
25351137962202521
CNPJ
15648426000204
Company information
Registration Holder
TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA
Manufacturer
TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Nov 24, 2025
Status
Active
About this record

Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81733730024 and manufactured by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA. The registration is held by TRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA with validity until Nov 24, 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.