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DEMAX Coronary Angiography Catheter - Indonesia BPOM Medical Device Registration

DEMAX Coronary Angiography Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420562. The device is manufactured by TIANJIN DEMAX MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PURE SOUTHEAST ASIA INDONESIA.

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 : C
DEMAX Coronary Angiography Catheter
Analysis ID: AKL 20501420562

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PURE SOUTHEAST ASIA INDONESIA

AR Address

Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman

Registration Date

Oct 18, 2024

Expiry Date

Mar 22, 2029

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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