ANVISA registration 80254180479Valid until Apr 07, 2035HAEMOPHILUS SP
ANVISA Registration Number: 80254180479PHADIA DIAGNOSTICOS LTDAOXOID LIMITEDRisk Class III
Device names
- Commercial name
- Família discos impregnados com agentes antimicrobianos isolados - Haemophilus
- Risk class
- Class III
Registration details
- Registration Number
- 80254180479
- Process Number
- 25351448327202495
- CNPJ
- 04930429000139
Company information
- Registration Holder
- PHADIA DIAGNOSTICOS LTDA
- Manufacturer
- OXOID LIMITED
- Manufacturing Country
- United Kingdom
PT: REINO UNIDO
Dates and status
- Publication Date
- Apr 07, 2025
- Validity
- 07/04/2035
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for HAEMOPHILUS SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180479 and manufactured by OXOID LIMITED. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Apr 07, 2035.
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.