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BONE RODS - ANVISA Registration 80203020071

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 80203020071 and manufactured by manufacturer not specified. The registration is held by BONE SURGICAL EQUIPAMENTOS MEDICOS LTDA with validity until Nov 25, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.

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80203020071
2 Related Devices
Registration Details
ANVISA Registration Number: 80203020071
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Related Devices (2)

Haste Intramedular de Fêmur Eba One
Risk Class III

Registration Details

80203020071

25351742747202384

04408009000197

Company Information

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01

Haste Intramedular de Fêmur Eba One
Risk Class III

Registration Details

80203020071

25351742747202384

04408009000197

Company Information

CITIEFFE S.R.L
Italy
PT: ITÁLIA

Dates and Status

Nov 25, 2024

25/11/2034

09/18/2025 19:00:01