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HONGDU Biphasic Defibrilator - Indonesia BPOM Medical Device Registration

HONGDU Biphasic Defibrilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505021573. The device is manufactured by JIANGSU HONGDU MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ARITEK KARYA MANDIRI.

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
HONGDU Biphasic Defibrilator
Analysis ID: AKL 20505021573

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ARITEK KARYA MANDIRI

AR Address

Green Lake City Rukan Crown Blok. A No. 19 Kelurahan Petir, Kecamatan Cipondoh Tangerang, Banten

Registration Date

Oct 16, 2023

Expiry Date

Oct 08, 2025

Product Type

Therapeutic Cardiology Equipment

DC-defribrillator (including paddles)

Non Radiation Electromedics

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