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ANVISA registration 80624969004Active

VACUUM WOUND THERAPY SYSTEM

ANVISA Registration Number: 80624969004K.C.I. BRASIL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS PARA A SAÚDE LTDAKCI USA, INC.Risk Class II
Device names
Technical name
VACUUM WOUND THERAPY SYSTEM
PT: SISTEMA A VÁCUO PARA TRATAMENTO DE FERIDAS
Commercial name
Unidade de Terapia PREVENA PLUS™ 125
Risk class
Class II
Registration details
Registration Number
80624969004
Process Number
25351367029202403
CNPJ
10918419000180
Company information
Manufacturer
KCI USA, INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 26, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for VACUUM WOUND THERAPY SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80624969004 and manufactured by KCI USA, INC.. The registration is held by K.C.I. BRASIL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS PARA A SAÚDE LTDA with validity until currently active (VIGENTE).

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