ANVISA registration 10216719033ActiveElectrode Removal Device
ANVISA Registration Number: 10216719033PHILIPS MEDICAL SYSTEMS LTDAPHILIPS IMAGE GUIDED THERAPY CORPORATIONRisk Class II
Device names
- Technical name
- Electrode Removal Device
- Commercial name
- Dispositivo de travamento de cabos-eletrodos - LLD
- Risk class
- Class II
PT: Dispositivo para Remocao de Eletrodo
Registration details
- Registration Number
- 10216719033
- Process Number
- 25351036324202593
- CNPJ
- 58295213000178
Company information
- Registration Holder
- PHILIPS MEDICAL SYSTEMS LTDA
- Manufacturer
- PHILIPS IMAGE GUIDED THERAPY CORPORATION
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Apr 07, 2025
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Electrode Removal Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10216719033 and manufactured by PHILIPS IMAGE GUIDED THERAPY CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until currently active (VIGENTE).
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