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GE Reusable ECG Electrodes - Indonesia BPOM Medical Device Registration

GE Reusable ECG Electrodes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502911516. The device is manufactured by SHENZHEN LAUNCH ELECTRICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS 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 : B
GE Reusable ECG Electrodes
Analysis ID: AKL 20502911516

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430

Registration Date

Aug 17, 2023

Expiry Date

Jun 19, 2028

Product Type

Monitoring Cardiology Equipment

Electrocardiograph electrode.

Non Electromedic Non Sterile

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