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ANVISA registration 81130100056Valid until Mar 30, 2036

Endoscopic electrosurgical electrode, bipolar, single use

ANVISA Registration Number: 81130100056VOLMED BRASIL EQUIPAMENTOS LTDA - MEVOLMED BRASIL EQUIPAMENTOS LTDA - MERisk Class III
Verified
Device names
Technical name
Endoscopic electrosurgical electrode, bipolar, single use
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PT: Eletrodo eletrocirúrgico endoscópico, bipolar, uso único
Commercial name
Pinça Bipolar Power Cut
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Risk class
Class III
Registration details
Registration Number
81130100056
Process Number
25351011938202643
CNPJ
20137275000189
Company information
Registration Holder
VOLMED BRASIL EQUIPAMENTOS LTDA - ME
Manufacturer
VOLMED BRASIL EQUIPAMENTOS LTDA - ME
Manufacturing Country
Brazil
PT: BRASIL
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 Endoscopic electrosurgical electrode, bipolar, single use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81130100056 and manufactured by VOLMED BRASIL EQUIPAMENTOS LTDA - ME. The registration is held by VOLMED BRASIL EQUIPAMENTOS LTDA - ME 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.