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SOLUTION FOR INTRA-ARTICULAR FILLING - ANVISA Registration 81050760120

Access comprehensive regulatory information for SOLUTION FOR INTRA-ARTICULAR FILLING in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81050760120 and manufactured by CROMA-PHARMA GMBH. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until Mar 29, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including DMC IMPORTACAO E EXPORTACAO DE EQUIPAMENTOS LTDA., FIDIA FARMACEUTICI S.P.A, 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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81050760120
2 Related Devices
Registration Details
ANVISA Registration Number: 81050760120
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Related Devices (2)

Ácido Hialurônico Sinovial – Kyeron Synoz
Risk Class IV

Registration Details

81050760120

25351963714202023

19443457000107

Company Information

CROMA-PHARMA GMBH
Austria
PT: ÁUSTRIA

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01

Ácido Hialurônico Sinovial – Kyeron Synoz
Risk Class IV

Registration Details

81050760120

25351963714202023

19443457000107

Dates and Status

Mar 29, 2021

29/03/2031

09/18/2025 19:00:01