ANVISA registration 80022060117Valid until Jun 16, 2035

BILIARY STENT

Name: BILIARY STENT — ANVISA registration 80022060117
Creator: FUJIFILM MEDWORK GMBH
Keywords: BILIARY STENT, STENT BILIAR, Stent Biliar PRO1, 80022060117, Risk Class III, ANVISA registration

ANVISA Registration Number: 80022060117FUJIFILM DO BRASIL LTDAFUJIFILM MEDWORK GMBHRisk Class III

Verified

Device names

Technical name: BILIARY STENT
Commercial name: Stent Biliar PRO1
Risk class: Class III

Registration details

Registration Number: 80022060117
Process Number: 25351366197202473
CNPJ: 60397874000156

Company information

Registration Holder: FUJIFILM DO BRASIL LTDA
Manufacturer: FUJIFILM MEDWORK GMBH
Manufacturing Country: Germany

Dates and status

Publication Date: Jun 16, 2025
Validity: 16/06/2035
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for BILIARY STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80022060117 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL LTDA with validity until Jun 16, 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.