Implantable Infusion Pump - ANVISA Registration 80182360003

Access comprehensive regulatory information for Implantable Infusion Pump in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80182360003 and manufactured by TRICUMED MEDIZINTECHNIK GMBH. The registration is held by Delta Medical Comercial Ltda with validity until Apr 22, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including MEDTRONIC, INC., and 2 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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80182360003
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Registration Details
ANVISA Registration Number: 80182360003
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Related Devices (2)

BOMBA DE INFUSÃO IMPLANTÁVEL DE FLUXO CONTÍNUO
Risk Class IV

Registration Details

80182360003

25351038496200809

04380711000190

Company Information

Germany
PT: ALEMANHA

Dates and Status

Apr 22, 2008

22/04/2028

09/18/2025 19:00:01

BOMBA DE INFUSÃO IMPLANTÁVEL DE FLUXO CONTÍNUO
Risk Class IV

Registration Details

80182360003

25351038496200809

04380711000190

Company Information

Dates and Status

Apr 22, 2008

22/04/2028

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "Implantable Infusion Pump"