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DEVICE FOR NEUROSURGERY - ANVISA Registration 81836600003

Access comprehensive regulatory information for DEVICE FOR NEUROSURGERY in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81836600003 and manufactured by PHENOX LIMITED. The registration is held by PHENOX DO BRASIL COMERCIO DE MATERIAS MEDICOS LTDA with validity until Dec 16, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDTRONIC, INC., SPES MEDICA S.R.L, 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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81836600003
2 Related Devices
Registration Details
ANVISA Registration Number: 81836600003
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Related Devices (2)

DISPOSITIVO DE TROMBECTOMIA pRESET LITE
Risk Class IV

Registration Details

81836600003

25351624522202347

33038158000100

Company Information

PHENOX LIMITED
Ireland
PT: IRLANDA

Dates and Status

Dec 16, 2024

16/12/2034

09/18/2025 19:00:01

DISPOSITIVO DE TROMBECTOMIA pRESET LITE
Risk Class IV

Registration Details

81836600003

25351624522202347

33038158000100

Company Information

Dates and Status

Dec 16, 2024

16/12/2034

09/18/2025 19:00:01