BONE RODS - ANVISA Registration 80203020019

Access comprehensive regulatory information for BONE RODS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80203020019 and manufactured by CITIEFFE S.R.L. The registration is held by BONE SURGICAL EQUIPAMENTOS MEDICOS LTDA with validity until Feb 22, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including NEOORTHO PRODUTOS ORTOPÉDICOS S/A, SYNTHES GMBH (OBERDORF), 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
80203020019
2 Related Devices
Registration Details
ANVISA Registration Number: 80203020019
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

Related Devices (2)

HASTE INTRAMEDULAR DE UMERO
Risk Class III

Registration Details

80203020019

25351209136200910

04408009000197

Company Information

CITIEFFE S.R.L
Italy
PT: ITÁLIA

Dates and Status

Feb 22, 2011

22/02/2026

09/18/2025 19:00:01

HASTE INTRAMEDULAR DE UMERO
Risk Class III

Registration Details

80203020019

25351209136200910

04408009000197

Company Information

Dates and Status

Feb 22, 2011

22/02/2026

09/18/2025 19:00:01