ANVISA registration 80012280214Valid until Aug 01, 2032INTRAVASCULAR GUIDE CATHETER
ANVISA Registration Number: 80012280214TERUMO MEDICAL DO BRASIL LTDA.TERUMO CORPORATIONRisk Class IV
Device names
- Technical name
- INTRAVASCULAR GUIDE CATHETER
- Commercial name
- Radifocus Glidecath Cateter Angiográfico Terumo 5Fr
- Risk class
- Class IV
PT: CATETER GUIA INTRAVASCULAR
Registration details
- Registration Number
- 80012280214
- Process Number
- 25351150603202216
- CNPJ
- 03129105000133
Company information
- Registration Holder
- TERUMO MEDICAL DO BRASIL LTDA.
- Manufacturer
- TERUMO CORPORATION
- Manufacturing Country
- Japan
PT: JAPÃO
Dates and status
- Publication Date
- Aug 01, 2022
- Validity
- 01/08/2032
- 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 80012280214 and manufactured by TERUMO CORPORATION. The registration is held by TERUMO MEDICAL DO BRASIL LTDA. with validity until Aug 01, 2032.
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