SPACER - ANVISA Registration 81382710002

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 81382710002 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 similar products found using AI-powered semantic search, 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 Similar Products
5 Competitors
81382710002
Registration Details
ANVISA Registration Number: 81382710002
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

SPACEFLUX
Risk Class I

Registration Details

81382710002

25351499633201922

92833946000157

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 05, 2019

VIGENTE

09/18/2025 19:00:01