ANVISA registration 81251089027ActiveGENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
ANVISA Registration Number: 81251089027ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDAMEDITECH DEVICES PVT LTDRisk Class II
Device names
- Technical name
- GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
- Risk class
- Class II
PT: FIO GUIA DE USO GERAL, NÃO VASCULAR
Registration details
- Registration Number
- 81251089027
- Process Number
- 25351084179202638
- CNPJ
- 21368015000187
Company information
- Registration Holder
- ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDA
- Manufacturer
- MEDITECH DEVICES PVT LTD
- Manufacturing Country
- India
PT: ÍNDIA
Dates and status
- Publication Date
- Jun 01, 2026
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
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 81251089027 and manufactured by MEDITECH DEVICES PVT LTD. The registration is held by ENDOSURG INDUSTRIA, COMERCIO, IMPORTACAO DISTRIBUICAO E LOCACAO DE MATERIAIS MEDICOS LTDA with validity until currently active (VIGENTE).
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