Endoscopic electrosurgical electrode, bipolar, single use
ANVISA Registration Number: 81130100057VOLMED BRASIL EQUIPAMENTOS LTDA - MEVOLMED BRASIL EQUIPAMENTOS LTDA - MERisk Class III
Device names
- Technical name
- Endoscopic electrosurgical electrode, bipolar, single use
- Risk class
- Class III
PT: Eletrodo eletrocirúrgico endoscópico, bipolar, uso único
Registration details
- Registration Number
- 81130100057
- Process Number
- 25351011949202623
- 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 81130100057 and manufactured by VOLMED BRASIL EQUIPAMENTOS LTDA - ME. The registration is held by VOLMED BRASIL EQUIPAMENTOS LTDA - ME with validity until Mar 30, 2036.
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