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

Lumbar decompression kit - ANVISA Registration 81637610133

Access comprehensive regulatory information for Lumbar decompression kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81637610133 and manufactured by Humanna Medical Ltda. The registration is held by Humanna Medical Ltda with validity until Mar 24, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME, MARDEN MEDICAL LTDA, 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
81637610133
Registration Details
ANVISA Registration Number: 81637610133
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit Cânula SkySafe
Risk Class III

Registration Details

81637610133

25351002385202557

27617206000111

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 24, 2025

24/03/2035

09/18/2025 19:00:01