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GE Definium XR120 - Indonesia BPOM Medical Device Registration

GE Definium XR120 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501918056. The device is manufactured by RAYENCE CO., LTD. from Korea, 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
GE Definium XR120
Analysis ID: AKL 21501918056

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

RAYENCE CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8

Registration Date

Jul 30, 2024

Expiry Date

May 16, 2029

Product Type

Diagnostic Radiology Equipment

Solid State X-Ray Imager (Flat Panel/Digital Imager)

Non Radiation Electromedics

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