ANVISA registration 80102513670ActiveANTICORPO PARA VÍRUS DE T-LINFOTRÓPICO HUMANO 1 E 2 (HTLV1 E HTLV2)
ANVISA Registration Number: 80102513670VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAAUTOBIO DIAGNOSTICS CO., LTDRisk Class IV
Device names
- Technical name
- ANTICORPO PARA VÍRUS DE T-LINFOTRÓPICO HUMANO 1 E 2 (HTLV1 E HTLV2)
- Commercial name
- Família AutoLumo Anti-HTLV Micropartículas (CLIA)
- Risk class
- Class IV
Registration details
- Registration Number
- 80102513670
- Process Number
- 25351099759202549
- CNPJ
- 04718143000194
Company information
- Registration Holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
- Manufacturer
- AUTOBIO DIAGNOSTICS CO., LTD
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Apr 22, 2026
- Status
- Active
About this record
Access comprehensive regulatory information for ANTICORPO PARA VÍRUS DE T-LINFOTRÓPICO HUMANO 1 E 2 (HTLV1 E HTLV2) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80102513670 and manufactured by AUTOBIO DIAGNOSTICS CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 22, 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.