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ANVISA registration 80013980038Valid until Apr 27, 2035

Material for Root Canal Disinfection and Obturation

ANVISA Registration Number: 80013980038F & A LABORATÓRIO FARMACÊUTICO LTDA-MEF & A LABORATÓRIO FARMACÊUTICO LTDA-MERisk Class IV
Verified
Device names
Technical name
Material for Root Canal Disinfection and Obturation
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PT: Material P/Desinfeccao e Obturacao Canal Radicular
Commercial name
FEAPEX - FÓRMULA & AÇÃO
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Risk class
Class IV
Registration details
Registration Number
80013980038
Process Number
25351669073201412
CNPJ
01953085000195
Company information
Registration Holder
F & A LABORATÓRIO FARMACÊUTICO LTDA-ME
Manufacturer
F & A LABORATÓRIO FARMACÊUTICO LTDA-ME
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Apr 27, 2015
Validity
27/04/2035
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Material for Root Canal Disinfection and Obturation in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80013980038 and manufactured by F & A LABORATÓRIO FARMACÊUTICO LTDA-ME. The registration is held by F & A LABORATÓRIO FARMACÊUTICO LTDA-ME with validity until Apr 27, 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.