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ANVISA registration 82249100023Valid until Jul 13, 2036

Endoscopic electrosurgical electrode, bipolar, single use

ANVISA Registration Number: 82249100023O-LINKE MEDICAL S.AO-LINKE MEDICAL S.ARisk 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
Eletrodos Bipolares flexível O-LINKE D2.7mm
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Risk class
Class III
Registration details
Registration Number
82249100023
Process Number
25351165135202527
CNPJ
40021197000160
Company information
Registration Holder
O-LINKE MEDICAL S.A
Manufacturer
O-LINKE MEDICAL S.A
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jul 13, 2026
Validity
13/07/2036
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 82249100023 and manufactured by O-LINKE MEDICAL S.A. The registration is held by O-LINKE MEDICAL S.A with validity until Jul 13, 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.