ANVISA registration 80462969010Active

Extension Tube

Name: Extension Tube — ANVISA registration 80462969010
Creator: CARDEA GMBH & CO. KG
Keywords: Extension Tube, Extensor, TRANSAFLOW MULTI 24HS, 80462969010, Risk Class II, ANVISA registration

ANVISA Registration Number: 80462969010PRONTOFAR LTDACARDEA GMBH & CO. KGRisk Class II

Verified

Device names

Technical name: Extension Tube
Commercial name: TRANSAFLOW MULTI 24HS
Risk class: Class II

Registration details

Registration Number: 80462969010
Process Number: 25351031808202546
CNPJ: 00098242000160

Company information

Registration Holder: PRONTOFAR LTDA
Manufacturer: CARDEA GMBH & CO. KG
Manufacturing Country: Germany

Dates and status

Publication Date: Mar 17, 2025
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for Extension Tube in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80462969010 and manufactured by CARDEA GMBH & CO. KG. The registration is held by PRONTOFAR LTDA with validity until currently active (VIGENTE).

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