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FOURIER M2-Upper Limb Rehabilitation Auxiliary Equipment - Indonesia BPOM Medical Device Registration

FOURIER M2-Upper Limb Rehabilitation Auxiliary Equipment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403918367. The device is manufactured by SHANGHAI FOURIER INTELLIGENCE CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AIRINDO MEDIKA CENTER.

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BPOM Registered
Risk Class Kelas Resiko : B
FOURIER M2-Upper Limb Rehabilitation Auxiliary Equipment
Analysis ID: AKL 21403918367

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. AIRINDO MEDIKA CENTER

AR Address

Jl. Teuku Nyak Arif No. 10, Simprug Galery Unit I, Kebayoran Lama

Registration Date

Dec 20, 2019

Expiry Date

Jun 07, 2024

Product Type

Therapeutic Physical Health Equipment

Powered exercise equipment.

Non Radiation Electromedics

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