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ANVISA registration 10338930359Valid until Aug 10, 2036

TREPONEMA PALLIDUM

ANVISA Registration Number: 10338930359EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDAEUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AGRisk Class IV
Verified
Device names
Technical name
TREPONEMA PALLIDUM
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Commercial name
Anti-Treponema pallidum ELISA 2.0 (IgGM)
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Risk class
Class IV
Registration details
Registration Number
10338930359
Process Number
25351056175202660
CNPJ
93741726000166
Company information
Registration Holder
EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA
Manufacturer
EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Aug 10, 2026
Validity
10/08/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for TREPONEMA PALLIDUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10338930359 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Aug 10, 2036.

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.