Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

VACUUM WOUND THERAPY SYSTEM - ANVISA Registration 80624969002

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 80624969002 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).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including KCI USA, INC., SMITH & NEPHEW MEDICAL LTD, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80624969002
Registration Details
ANVISA Registration Number: 80624969002
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Sistema de Controle de incisões PREVENA PLUS™
Risk Class II

Registration Details

80624969002

25351605259202125

10918419000180

Company Information

KCI USA, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 17, 2021

VIGENTE

09/18/2025 19:00:01