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ANVISA registration 10356330031Active

Ear impression material

ANVISA Registration Number: 10356330031CENTRO AUDITIVO MICROSOM LTDA .DREVE-OTOPLASTIK GMBHRisk Class I
Verified
Device names
Technical name
Ear impression material
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PT: Material de moldagem auricular
Commercial name
MASSA DE PRÉ-MOLDAGEM AURICULAR
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Risk class
Class I
Registration details
Registration Number
10356330031
Process Number
25351560769200909
CNPJ
66704701000110
Company information
Registration Holder
CENTRO AUDITIVO MICROSOM LTDA .
Manufacturer
DREVE-OTOPLASTIK GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Dec 26, 2011
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Ear impression material in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10356330031 and manufactured by DREVE-OTOPLASTIK GMBH. The registration is held by CENTRO AUDITIVO MICROSOM 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.