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CARDIOSOFT - Indonesia BPOM Medical Device Registration

CARDIOSOFT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320685. The device is manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
CARDIOSOFT
Analysis ID: AKL 20501320685

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430

Registration Date

Feb 21, 2024

Expiry Date

Mar 22, 2026

Product Type

Diagnostic Cardiology Equipment

Programmable diagnostic computer.

Non Radiation Electromedics

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