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ANVISA registration 80012280094Active

Guide Wire

ANVISA Registration Number: 80012280094TERUMO MEDICAL DO BRASIL LTDA.VASCUTEK LIMITEDRisk Class IV
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA ANACONDA TERUMO
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Risk class
Class IV
Registration details
Registration Number
80012280094
Process Number
25351042336200856
CNPJ
03129105000133
Company information
Registration Holder
TERUMO MEDICAL DO BRASIL LTDA.
Manufacturer
VASCUTEK LIMITED
Manufacturing Country
United Kingdom
PT: REINO UNIDO
Dates and status
Publication Date
Mar 10, 2008
Status
Active
About this record

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80012280094 and manufactured by VASCUTEK LIMITED. The registration is held by TERUMO MEDICAL DO BRASIL LTDA. with validity until Mar 10, 2028.

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.