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CU-HD 1 Defibrillator - Indonesia BPOM Medical Device Registration

CU-HD 1 Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505220018. The device is manufactured by CU MEDICAL SYSTEM, INC from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.

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
CU-HD 1 Defibrillator
Analysis ID: AKL 30505220018

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. GLOBAL MEDICAL PRESS

AR Address

Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

Jan 08, 2025

Expiry Date

Dec 01, 2027

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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