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ANVISA registration 10212990279Active

GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR

ANVISA Registration Number: 10212990279E TAMUSSINO E CIA LTDACOOK ENDOSCOPYRisk Class II
Device names
Technical name
GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
PT: FIO GUIA DE USO GERAL, NÃO VASCULAR
Commercial name
FIO GUIA BILIAR FUSION
Risk class
Class II
Registration details
Registration Number
10212990279
Process Number
25351676728200972
CNPJ
33100082000103
Company information
Registration Holder
E TAMUSSINO E CIA LTDA
Manufacturer
COOK ENDOSCOPY
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 19, 2010
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10212990279 and manufactured by COOK ENDOSCOPY. The registration is held by E TAMUSSINO E CIA 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.