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Single-use cardiac electrophysiology catheter - ANVISA Registration 10332340514

Access comprehensive regulatory information for Single-use cardiac electrophysiology catheter in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10332340514 and manufactured by ABBOTT MEDICAL. The registration is held by ST. JUDE MEDICAL BRASIL LTDA. with validity until Jul 21, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SHANGHAI MICROPORT EP MEDTECH CO., LTD, 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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10332340514
2 Related Devices
Registration Details
ANVISA Registration Number: 10332340514
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Related Devices (2)

Cateter para Eletrofisiologia Direcionável Livewire
Risk Class IV

Registration Details

10332340514

25351074374202579

00986846000142

Company Information

ABBOTT MEDICAL
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 21, 2025

21/07/2035

09/18/2025 19:00:01

Cateter para Eletrofisiologia Direcionável Livewire
Risk Class IV

Registration Details

10332340514

25351074374202579

00986846000142

Company Information

Dates and Status

Jul 21, 2025

21/07/2035

09/18/2025 19:00:01