ANVISA registration 81506640019ActiveGENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
ANVISA Registration Number: 81506640019ONCORMED PRODUTOS PARA SAÚDE LTDA - MEBIÇAKCILAR TIBBI CIHAZLAR SANAYI A.S.Risk Class I
Device names
- Technical name
- GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
- Risk class
- Class I
PT: FIO GUIA DE USO GERAL, NÃO VASCULAR
Registration details
- Registration Number
- 81506640019
- Process Number
- 25351440722202187
- CNPJ
- 20088885000130
Company information
- Registration Holder
- ONCORMED PRODUTOS PARA SAÚDE LTDA - ME
- Manufacturer
- BIÇAKCILAR TIBBI CIHAZLAR SANAYI A.S.
- Manufacturing Country
- Türkiye
PT: TURQUIA
Dates and status
- Publication Date
- May 13, 2021
- 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 I medical device is registered under ANVISA number 81506640019 and manufactured by BIÇAKCILAR TIBBI CIHAZLAR SANAYI A.S.. The registration is held by ONCORMED PRODUTOS PARA SAÚDE LTDA - ME with validity until currently active (VIGENTE).
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