ANVISA registration 81022030024Active

Instrument Kit

Name: Instrument Kit — ANVISA registration 81022030024
Creator: SINTEA PLUSTEK S.R.L.
Keywords: Instrument Kit, Kit Instrumental, INSTRUMENTAL PARA SISTEMA LOMBAR POSTERIOR, 81022030024, Risk Class I, ANVISA registration

ANVISA Registration Number: 81022030024SOLLIEVO MEDICINA ESPECIALIZADA LTDASINTEA PLUSTEK S.R.L.Risk Class I

Verified

Device names

Technical name: Instrument Kit
Commercial name: INSTRUMENTAL PARA SISTEMA LOMBAR POSTERIOR
Risk class: Class I

Registration details

Registration Number: 81022030024
Process Number: 25351203836201719
CNPJ: 18797208000149

Company information

Registration Holder: SOLLIEVO MEDICINA ESPECIALIZADA LTDA
Manufacturer: SINTEA PLUSTEK S.R.L.
Manufacturing Country: Italy

Dates and status

Publication Date: May 17, 2017
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81022030024 and manufactured by SINTEA PLUSTEK S.R.L.. The registration is held by SOLLIEVO MEDICINA ESPECIALIZADA LTDA with validity until currently active (VIGENTE).

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