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DUAL CHAMBER IMPLANTABLE DEFIBRILLATOR - ANVISA Registration 10349001212

Access comprehensive regulatory information for DUAL CHAMBER IMPLANTABLE DEFIBRILLATOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10349001212 and manufactured by manufacturer not specified. The registration is held by AUTO SUTURE DO BRASIL LTDA. with validity until Feb 13, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BIOTRONIK SE & CO. KG, ABBOTT MEDICAL, 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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10349001212
2 Related Devices
Registration Details
ANVISA Registration Number: 10349001212
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Related Devices (2)

CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL - PROTECTA
Risk Class IV

Registration Details

10349001212

25351469217202114

01645409000128

Company Information

Dates and Status

May 24, 2021

13/02/2028

09/18/2025 19:00:01

CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL - PROTECTA
Risk Class IV

Registration Details

10349001212

25351469217202114

01645409000128

Company Information

MEDTRONIC INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 24, 2021

13/02/2028

09/18/2025 19:00:01