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ANVISA registration 10338930243Active

REVERSE TRIIODOTHYRONINE (T3)

ANVISA Registration Number: 10338930243EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDAEUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDARisk Class II
Verified
Device names
Technical name
REVERSE TRIIODOTHYRONINE (T3)
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PT: TRIIODOTIRONINA (T3) REVERSA
Commercial name
T3 Reversa
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Risk class
Class II
Registration details
Registration Number
10338930243
Process Number
25351467560202043
CNPJ
93741726000166
Company information
Registration Holder
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
Manufacturer
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Dec 10, 2020
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for REVERSE TRIIODOTHYRONINE (T3) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10338930243 and manufactured by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA 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.