ANVISA registration 10300390827ActiveANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM)
ANVISA Registration Number: 10300390827VYTTRA DIAGNOSTICOS S.A.DR. FOOKE LABORATORIEN GMBHRisk Class II
Device names
- Technical name
- ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM)
- Risk class
- Class II
PT: ANTICORPO ANTIMEMBRANA BASAL GLOMERULAR (GMB)
Registration details
- Registration Number
- 10300390827
- Process Number
- 25351253374201995
- CNPJ
- 00904728000148
Company information
- Registration Holder
- VYTTRA DIAGNOSTICOS S.A.
- Manufacturer
- DR. FOOKE LABORATORIEN GMBH
- Manufacturing Country
- Germany
PT: ALEMANHA
Dates and status
- Publication Date
- Jul 08, 2019
- Status
- Active
Official value: VIGENTE
About this record
Access comprehensive regulatory information for ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10300390827 and manufactured by DR. FOOKE LABORATORIEN GMBH. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until currently active (VIGENTE).
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