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Treatment Planning Software For Radiotherapy - ANVISA Registration 10361700010

Access comprehensive regulatory information for Treatment Planning Software For Radiotherapy in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10361700010 and manufactured by PROWESS INC.. The registration is held by OXIGEN COMERCIO, INDUSTRIA E REPRESENTACOES DE EQUIPAMENTOS MEDICOS LTDA - EPP with validity until Jul 30, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including VARIAN MEDICAL SYSTEMS, INC., NUCLETRON B.V., 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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10361700010
2 Related Devices
Registration Details
ANVISA Registration Number: 10361700010
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Related Devices (2)

SOFTWARE DE PLANEJAMENTO DE TRATAMENTO DE RADIACAO PROWESS PANTHER
Risk Class III

Registration Details

10361700010

25351069025200753

00911246000115

Company Information

PROWESS INC.
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Jul 30, 2007

30/07/2027

09/18/2025 19:00:01

SOFTWARE DE PLANEJAMENTO DE TRATAMENTO DE RADIACAO PROWESS PANTHER
Risk Class III

Registration Details

10361700010

25351069025200753

00911246000115

Dates and Status

Jul 30, 2007

30/07/2027

09/18/2025 19:00:01