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ANVISA registration 80254180475Valid until Mar 05, 2035

CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)

ANVISA Registration Number: 80254180475PHADIA DIAGNOSTICOS LTDAOXOID LIMITEDRisk Class III
Verified
Device names
Technical name
CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE)
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Commercial name
ProSpecT C. difficile Toxin A/B Microplate Assay
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Risk class
Class III
Registration details
Registration Number
80254180475
Process Number
25351434052202411
CNPJ
04930429000139
Company information
Registration Holder
PHADIA DIAGNOSTICOS LTDA
Manufacturer
OXOID LIMITED
Manufacturing Country
United Kingdom
PT: REINO UNIDO
Dates and status
Publication Date
Mar 05, 2025
Validity
05/03/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CLOSTRIDIUM DIFFICILE (CLOSTRIDIOIDES DIFFICILE) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180475 and manufactured by OXOID LIMITED. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Mar 05, 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.