DEHYDROEPIANDROSTERONE (DHEA)
ANVISA Registration Number: 81905510079GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDADRG INSTRUMENTS GMBHRisk Class II
Device names
- Technical name
- DEHYDROEPIANDROSTERONE (DHEA)
- Risk class
- Class II
PT: DEHIDROEPIANDROSTERONA (DHEA)
Registration details
- Registration Number
- 81905510079
- Process Number
- 25351209055202329
- CNPJ
- 34255136000164
Company information
- Registration Holder
- GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDA
- Manufacturer
- DRG INSTRUMENTS GMBH
- Manufacturing Country
- Germany
PT: ALEMANHA
Dates and status
- Publication Date
- May 08, 2023
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for DEHYDROEPIANDROSTERONE (DHEA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81905510079 and manufactured by DRG INSTRUMENTS GMBH. The registration is held by GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).
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