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ANVISA registration 80633660030Valid until Mar 30, 2036

Debrider

ANVISA Registration Number: 80633660030IGI COMERCIO DE EQUIPAMENTOS ELETRONICOS LTDAACTO GMBHRisk Class IV
Verified
Device names
Technical name
Debrider
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PT: Debridador
Commercial name
Actolind® w Gel
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Risk class
Class IV
Registration details
Registration Number
80633660030
Process Number
25351043811202511
CNPJ
10394359000144
Company information
Registration Holder
IGI COMERCIO DE EQUIPAMENTOS ELETRONICOS LTDA
Manufacturer
ACTO GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Mar 30, 2026
Validity
30/03/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Debrider in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80633660030 and manufactured by ACTO GMBH. The registration is held by IGI COMERCIO DE EQUIPAMENTOS ELETRONICOS LTDA with validity until Mar 30, 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.