ANVISA registration 80770430015ActiveSelf-test instrument for glucose
ANVISA Registration Number: 80770430015DMAX - DISTRIBUIDORA DE MEDICAMENTOS E MATERIAL HOSPITALAR LTDA - EPPM.I. TECH CO., LTDRisk Class III
Device names
- Technical name
- Self-test instrument for glucose
- Risk class
- Class III
PT: Instrumento autoteste para glicose
Registration details
- Registration Number
- 80770430015
- Process Number
- 25351491693202031
- CNPJ
- 09390408000191
Company information
- Registration Holder
- DMAX - DISTRIBUIDORA DE MEDICAMENTOS E MATERIAL HOSPITALAR LTDA - EPP
- Manufacturer
- M.I. TECH CO., LTD
- Manufacturing Country
- South Korea
PT: CORÉIA DO SUL
Dates and status
- Publication Date
- Jan 04, 2021
- Status
- Active
About this record
Access comprehensive regulatory information for Self-test instrument for glucose in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80770430015 and manufactured by M.I. TECH CO., LTD. The registration is held by DMAX - DISTRIBUIDORA DE MEDICAMENTOS E MATERIAL HOSPITALAR LTDA - EPP with validity until Jan 04, 2031.
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