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ANVISA registration 80989250039Valid until May 18, 2036

Endoscopic electrosurgical electrode, bipolar, single use

ANVISA Registration Number: 80989250039R3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDAR3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDARisk 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
SPINEW™ Disc System for Endoscopic Discectomy
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Risk class
Class III
Registration details
Registration Number
80989250039
Process Number
25351037769202671
CNPJ
14697578000153
Company information
Registration Holder
R3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
R3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
May 18, 2026
Validity
18/05/2036
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 80989250039 and manufactured by R3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDA. The registration is held by R3A MEDICAL INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES LTDA with validity until May 18, 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.