ANVISA registration 80192019020ActivePhacoemulsification Kit
ANVISA Registration Number: 80192019020ADAPT PRODUTOS OFTALMOLÓGICOS LTDAOERTLI INSTRUMENTE AGRisk Class II
Device names
- Technical name
- Phacoemulsification Kit
- Commercial name
- MD0105.21 KIT DE ACESSÓRIOS DE FACOEMULSIFICAÇÃO OERTLI USO ÚNICO
- Risk class
- Class II
PT: Kit Para Facoemulsificacao
Registration details
- Registration Number
- 80192019020
- Process Number
- 25351052354202628
- CNPJ
- 96382429000160
Company information
- Registration Holder
- ADAPT PRODUTOS OFTALMOLÓGICOS LTDA
- Manufacturer
- OERTLI INSTRUMENTE AG
- Manufacturing Country
- Switzerland
PT: SUÍÇA
Dates and status
- Publication Date
- Mar 30, 2026
- Validity
- VIGENTE
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Phacoemulsification Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80192019020 and manufactured by OERTLI INSTRUMENTE AG. The registration is held by ADAPT PRODUTOS OFTALMOLÓGICOS LTDA with validity until currently active (VIGENTE).
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