ANVISA registration 80192019012Active

Surgical Kit

Name: Surgical Kit — ANVISA registration 80192019012
Creator: SIE SURGICAL INSTRUMENT ENGINEERING AG
Keywords: Surgical Kit, Kit Cirurgico, PROCEDURE PACK CATARACT CORNEAL SURGERY LIQUID, 80192019012, Risk Class II, ANVISA registration

ANVISA Registration Number: 80192019012ADAPT PRODUTOS OFTALMOLÓGICOS LTDASIE SURGICAL INSTRUMENT ENGINEERING AGRisk Class II

Verified

Device names

Technical name: Surgical Kit
Commercial name: PROCEDURE PACK CATARACT CORNEAL SURGERY LIQUID
Risk class: Class II

Registration details

Registration Number: 80192019012
Process Number: 25351024425202601
CNPJ: 96382429000160

Company information

Registration Holder: ADAPT PRODUTOS OFTALMOLÓGICOS LTDA
Manufacturer: SIE SURGICAL INSTRUMENT ENGINEERING AG
Manufacturing Country: Switzerland

Dates and status

Publication Date: Feb 18, 2026
Status: Active

About this record

Access comprehensive regulatory information for Surgical 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 80192019012 and manufactured by SIE SURGICAL INSTRUMENT ENGINEERING AG. The registration is held by ADAPT PRODUTOS OFTALMOLÓGICOS LTDA with validity until currently active (VIGENTE).

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