Pure Global AI
ANVISA registration 80224390320Valid until Feb 02, 2036

INTRAVASCULAR GUIDE CATHETER

ANVISA Registration Number: 80224390320BIOTRONIK COMERCIAL MÉDICA LTDA.IMDS OPERATIONS B.V.Risk Class IV
Verified
Device names
Technical name
INTRAVASCULAR GUIDE CATHETER
View exact technical-name matches →
PT: CATETER GUIA INTRAVASCULAR
Commercial name
GUIDION - CATETER GUIA DE EXTENSÃO CORONARIANO
View exact commercial-name matches →
Risk class
Class IV
Registration details
Registration Number
80224390320
Process Number
25351400898202449
CNPJ
50595271000105
Company information
Registration Holder
BIOTRONIK COMERCIAL MÉDICA LTDA.
Manufacturer
IMDS OPERATIONS B.V.
Manufacturing Country
Netherlands
PT: HOLANDA (PAÍSES BAIXOS)
Dates and status
Publication Date
Feb 02, 2026
Validity
02/02/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80224390320 and manufactured by IMDS OPERATIONS B.V.. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Feb 02, 2036.

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.