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ANVISA registration 80022069063Active

Infusion/injection devices

ANVISA Registration Number: 80022069063FUJIFILM DO BRASIL LTDAFUJIFILM MEDWORK GMBHRisk Class II
Verified
Device names
Technical name
Infusion/injection devices
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PT: Dispositivos de infusão/injeção
Commercial name
Cateter ERCP CAN1-S
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Risk class
Class II
Registration details
Registration Number
80022069063
Process Number
25351235528202513
CNPJ
60397874000156
Company information
Registration Holder
FUJIFILM DO BRASIL LTDA
Manufacturer
FUJIFILM MEDWORK GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Apr 27, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Infusion/injection devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80022069063 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL LTDA with validity until currently active (VIGENTE).

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.