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Bipolar Forceps - ANVISA Registration 80003890162

Access comprehensive regulatory information for Bipolar Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80003890162 and manufactured by manufacturer not specified. The registration is held by CANADA CENTRAL DE NEGOCIOS DO BRASIL LTDA with validity until Jun 17, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including euro parts brasil industria e comercio de instrumental cirurgico ltda, MB INDUSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA, 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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80003890162
2 Related Devices
Registration Details
ANVISA Registration Number: 80003890162
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Related Devices (2)

Pinça Bipolar EndoSafe Non Stick Tecno
Risk Class III

Registration Details

80003890162

25351175774202410

01911022000176

Company Information

Dates and Status

Jun 17, 2024

17/06/2034

09/18/2025 19:00:01

Pinça Bipolar EndoSafe Non Stick Tecno
Risk Class III

Registration Details

80003890162

25351175774202410

01911022000176

Company Information

Pakistan
PT: PAQUISTÃO

Dates and Status

Jun 17, 2024

17/06/2034

09/18/2025 19:00:01