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ANVISA registration 81807370001Valid until Feb 07, 2032

High Frequency Surgical Equipment

ANVISA Registration Number: 81807370001DERMITEK SYSTEM TECNOLOGIAS LTDADERMITEK SYSTEM TECNOLOGIAS LTDARisk Class III
Verified
Device names
Technical name
High Frequency Surgical Equipment
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PT: Equipamento Cirurgico de Alta Frequencia
Commercial name
Gerador Eletrocirúrgico Wise Surgeon®
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Risk class
Class III
Registration details
Registration Number
81807370001
Process Number
25351208023202144
CNPJ
30767266000125
Company information
Registration Holder
DERMITEK SYSTEM TECNOLOGIAS LTDA
Manufacturer
DERMITEK SYSTEM TECNOLOGIAS LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Feb 07, 2022
Validity
07/02/2032
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for High Frequency Surgical Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81807370001 and manufactured by DERMITEK SYSTEM TECNOLOGIAS LTDA. The registration is held by DERMITEK SYSTEM TECNOLOGIAS LTDA with validity until Feb 07, 2032.

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.