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i-PAD CU-SP2 - Indonesia BPOM Medical Device Registration

i-PAD CU-SP2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505028018. 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 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
i-PAD CU-SP2
Analysis ID: AKL 30505028018

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

GLOBAL MEDICAL PRESS

AR Address

Kompl.Green Garden AA-1/17 Jl.MH Thamrin KM 7 RT 04/RW 02 Kel.Panunggangan Utara Kec.Pinang.Kota Tangerang

Registration Date

Jan 29, 2022

Expiry Date

Jan 01, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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