ANVISA 82209520068Endoscopic electrosurgical electrode, bipolar, single use
ANVISA Registration Number: 82209520068 · MARDEN MEDICAL LTDA · MARDEN MEDICAL LTDA · Risk Class III · Valid until Aug 18, 2035
Device Details
Endoscopic electrosurgical electrode, bipolar, single use
- Registration Number
- 82209520068
- Process Number
- 25351086117202580
- CNPJ
- 40220751000138
- Registration Holder
- MARDEN MEDICAL LTDA
- Manufacturer
- MARDEN MEDICAL LTDA
- Manufacturing Country
- Brazil
- PT: BRASIL
- Publication Date
- Aug 18, 2025
- Validity
- 18/08/2035
- Last Updated
- 09/18/2025 19:00:01
- Manufacturer
- MARDEN MEDICAL LTDA
- Registration
- 82209520086
- Publication Date
- Sep 15, 2025
- Manufacturer
- MARDEN MEDICAL LTDA
- Registration
- 82209520087
- Publication Date
- Sep 15, 2025
- Manufacturer
- MARDEN MEDICAL LTDA
- Registration
- 82209520088
- Publication Date
- Sep 15, 2025
- Manufacturer
- MARDEN MEDICAL LTDA
- Registration
- 82209520081
- Publication Date
- Sep 08, 2025
- Manufacturer
- MARDEN MEDICAL LTDA
- Registration
- 82209520082
- Publication Date
- Sep 08, 2025
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 82209520068 and manufactured by MARDEN MEDICAL LTDA. The registration is held by MARDEN MEDICAL LTDA with validity until Aug 18, 2035.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.