Pure Global AI
ANVISA registration 10216710412Valid until Mar 16, 2036

INTRAVASCULAR GUIDE CATHETER

ANVISA Registration Number: 10216710412PHILIPS MEDICAL SYSTEMS LTDAPHILIPS IMAGE GUIDED THERAPY CORPORATIONRisk Class IV
Verified
Device names
Technical name
INTRAVASCULAR GUIDE CATHETER
View exact technical-name matches →
PT: CATETER GUIA INTRAVASCULAR
Commercial name
Cateter Digital IVUS Eagle Eye Platinum
View exact commercial-name matches →
Risk class
Class IV
Registration details
Registration Number
10216710412
Process Number
25351002768202614
CNPJ
58295213000178
Company information
Registration Holder
PHILIPS MEDICAL SYSTEMS LTDA
Manufacturer
PHILIPS IMAGE GUIDED THERAPY CORPORATION
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Mar 16, 2026
Validity
16/03/2036
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 10216710412 and manufactured by PHILIPS IMAGE GUIDED THERAPY CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Mar 16, 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.