ANVISA registration 80021290015Valid until Feb 07, 2032Solution For Ophthalmic Use
ANVISA Registration Number: 80021290015CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.Risk Class III
Device names
- Technical name
- Solution For Ophthalmic Use
- Commercial name
- LUNERA (carmelose sodica 0,5% + glicerol 0,9%) solução oftálmica
- Risk class
- Class III
PT: Solucao Para Uso Oftalmologico
Registration details
- Registration Number
- 80021290015
- Process Number
- 25351300046202118
- CNPJ
- 44734671000151
Company information
- Registration Holder
- CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.
- Manufacturer
- CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.
- Manufacturing Country
- Brazil
PT: BRASIL
Dates and status
- Publication Date
- Feb 07, 2022
- Validity
- 07/02/2032
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Solution For Ophthalmic Use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80021290015 and manufactured by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.. The registration is held by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA. with validity until Feb 07, 2032.
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