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

SPACER - ANVISA Registration 81382710001

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81382710001 and manufactured by ZANDEI INDUSTRIA DE PLASTICOS LTDA. The registration is held by ZANDEI INDUSTRIA DE PLASTICOS 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 PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA, HUIZHOU KAIYI TECHNOLOGY CO.,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
81382710001
Registration Details
ANVISA Registration Number: 81382710001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SPACEFLUX COM MÁSCARA
Risk Class I

Registration Details

81382710001

25351420793201949

92833946000157

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 01, 2019

VIGENTE

09/18/2025 19:00:01