ANVISA registration 82444370264ActivePROGESTERONE
ANVISA Registration Number: 82444370264Enzytec Biotecnologia Ltda.ZHEJIANG ORIENT GENE BIOTECH CO., LTD.Risk Class II
Device names
- Commercial name
- Família PROG Quantitative Test Kit (Time-Resolved FIA)
- Risk class
- Class II
Registration details
- Registration Number
- 82444370264
- Process Number
- 25351122629202517
- CNPJ
- 07214566000165
Company information
- Registration Holder
- Enzytec Biotecnologia Ltda.
- Manufacturer
- ZHEJIANG ORIENT GENE BIOTECH CO., LTD.
- Manufacturing Country
- China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
- Publication Date
- Sep 08, 2025
- Status
- Active
Official value: VIGENTE
About this record
Access comprehensive regulatory information for PROGESTERONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82444370264 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by Enzytec Biotecnologia 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.