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ANVISA registration 80313830005Active

DIFFERENTIAL CULTURE MEDIA AND DEVICES INTENDED FOR THE IDENTIFICATION OF MICROORGANISMS THROUGH BIOCHEMICAL TESTS

ANVISA Registration Number: 80313830005ASSOCIATES OF CAPE COD INTERNATIONAL-BRASIL LTDA.ASSOCIATES OF CAPE COD, INCRisk Class I
Verified
Device names
Technical name
DIFFERENTIAL CULTURE MEDIA AND DEVICES INTENDED FOR THE IDENTIFICATION OF MICROORGANISMS THROUGH BIOCHEMICAL TESTS
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PT: MEIOS DE CULTURA E DISPOSITIVOS DIFERENCIAIS DESTINADOS À IDENTIFICAÇÃO DE MICROORGANISMOS POR MEIO DE TESTES BIOQUÍMICOS
Commercial name
KIT PARA DETECÇÃO DO (1-3)- beta-D-GLUCANO NO SORO - FUNGITELL
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Risk class
Class I
Registration details
Registration Number
80313830005
Process Number
25351618184200875
CNPJ
04088991000167
Company information
Registration Holder
ASSOCIATES OF CAPE COD INTERNATIONAL-BRASIL LTDA.
Manufacturer
ASSOCIATES OF CAPE COD, INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Dec 22, 2008
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for DIFFERENTIAL CULTURE MEDIA AND DEVICES INTENDED FOR THE IDENTIFICATION OF MICROORGANISMS THROUGH BIOCHEMICAL TESTS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80313830005 and manufactured by ASSOCIATES OF CAPE COD, INC. The registration is held by ASSOCIATES OF CAPE COD INTERNATIONAL-BRASIL 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.