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GE Ultrasound pulsed doppler imaging system - Indonesia BPOM Medical Device Registration

GE Ultrasound pulsed doppler imaging system is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501817406. The device is manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES-CRITIKON DE MEXICO S. DE R.L. DE C.V from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GE Ultrasound pulsed doppler imaging system
Analysis ID: AKL 21501817406

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

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

May 24, 2022

Expiry Date

Mar 02, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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