ANVISA registration 81721489004ActivePatient Monitoring System
ANVISA Registration Number: 81721489004JRMEDIC -COMERCIO E ASSISTÊNCIA TÉCNICA LTDAMGC DIAGNOSTICS CORPORATIONRisk Class II
Device names
- Technical name
- Patient Monitoring System
- Commercial name
- Resmon PRO V3 - Dispositivo de Monitoração da Função Respiratória
- Risk class
- Class II
PT: Sistema de Monitoracao de Paciente
Registration details
- Registration Number
- 81721489004
- Process Number
- 25351963720202081
- CNPJ
- 03329477000103
Company information
- Registration Holder
- JRMEDIC -COMERCIO E ASSISTÊNCIA TÉCNICA LTDA
- Manufacturer
- MGC DIAGNOSTICS CORPORATION
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Oct 01, 2020
- Status
- Active
Official value: VIGENTE
About this record
Access comprehensive regulatory information for Patient Monitoring System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81721489004 and manufactured by MGC DIAGNOSTICS CORPORATION. The registration is held by JRMEDIC -COMERCIO E ASSISTÊNCIA TÉCNICA LTDA with validity until currently active (VIGENTE).
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.