ANVISA registration 80002670150ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 80002670150RENYLAB QUÍMICA E FARMACÊUTICA LTDALGM INTERNATIONAL, INC.Risk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 80002670150
- Process Number
- 25351042151202623
- CNPJ
- 00562583000144
Company information
- Registration Holder
- RENYLAB QUÍMICA E FARMACÊUTICA LTDA
- Manufacturer
- LGM INTERNATIONAL, INC.
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Apr 22, 2026
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80002670150 and manufactured by LGM INTERNATIONAL, INC.. The registration is held by RENYLAB QUÍMICA E FARMACÊUTICA 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.