ANVISA registration 81365089006ActiveDevice for intraocular lens implantation
ANVISA Registration Number: 81365089006vertek consumo clinico e hospitalar Ltda meYILMAZ MEDIKAL-MUSTAFA NAZLIERRisk Class II
Device names
- Technical name
- Device for intraocular lens implantation
- Commercial name
- SISTEMA DE CARTUCHO E INJETOR DE LENTE INTRAOCULAR
- Risk class
- Class II
PT: Dispositivo para implantação de lentes intra oculares
Registration details
- Registration Number
- 81365089006
- Process Number
- 25351014339202509
- CNPJ
- 22898875000195
Company information
- Registration Holder
- vertek consumo clinico e hospitalar Ltda me
- Manufacturer
- YILMAZ MEDIKAL-MUSTAFA NAZLIER
- Manufacturing Country
- Türkiye
PT: TURQUIA
Dates and status
- Publication Date
- Feb 10, 2025
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Device for intraocular lens implantation in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81365089006 and manufactured by YILMAZ MEDIKAL-MUSTAFA NAZLIER. The registration is held by vertek consumo clinico e hospitalar Ltda me with validity until currently active (VIGENTE).
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