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FOURIER HandyRehab ™ Hand Rehabilitation Equipment - Indonesia BPOM Medical Device Registration

FOURIER HandyRehab ™ Hand Rehabilitation Equipment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420310. The device is manufactured by ZUNOZAKI LIMITED from Hong Kong (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 HandyRehab ™ Hand Rehabilitation Equipment
Analysis ID: AKL 21403420310

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ZUNOZAKI LIMITED

Country of Origin

Hong Kong (China)

Authorized Representative

PT. AIRINDO MEDIKA CENTER

AR Address

Jalan Teuku Nyak Arief NO. 10

Registration Date

Aug 04, 2024

Expiry Date

Feb 06, 2028

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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