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

Bone Distractor - ANVISA Registration 10309310071

Access comprehensive regulatory information for Bone Distractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10309310071 and manufactured by MICRODENT APARELHOS MEDICOS E ODONTOLOGICOS LTDA - EPP. The registration is held by MICRODENT APARELHOS MEDICOS E ODONTOLOGICOS LTDA - EPP with validity until Oct 18, 2031.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ENGIMPLAN ENGENHARIA DE IMPLANTE IND E COM LTDA, TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP, 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
10309310071
Registration Details
ANVISA Registration Number: 10309310071
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Distrator Ósseo Cran-Max
Risk Class III

Registration Details

10309310071

25351300864202111

58061557000112

Company Information

Dates and Status

Oct 18, 2021

18/10/2031

09/18/2025 19:00:01