ANVISA registration 10298910183ActiveInstrumento para preparo e processamento de amostras fase pré-analítica
ANVISA Registration Number: 10298910183REVVITY DO BRASIL LTDAOMNI INTERNATIONAL, INCRisk Class I
Device names
- Technical name
- Instrumento para preparo e processamento de amostras fase pré-analítica
- Risk class
- Class I
Registration details
- Registration Number
- 10298910183
- Process Number
- 25351387280202486
- CNPJ
- 00351210000124
Company information
- Registration Holder
- REVVITY DO BRASIL LTDA
- Manufacturer
- OMNI INTERNATIONAL, INC
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Sep 16, 2024
- 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 10298910183 and manufactured by OMNI INTERNATIONAL, INC. The registration is held by REVVITY DO BRASIL LTDA with validity until currently active (VIGENTE).
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