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NUVA Flow Diverter - Indonesia BPOM Medical Device Registration

NUVA Flow Diverter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003420068. The device is manufactured by BEIJING TAIJIEWEIYE TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
NUVA Flow Diverter
Analysis ID: AKL 31003420068

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Aug 02, 2024

Expiry Date

Apr 15, 2026

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Electromedic Sterile

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