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FX 80 Classix - Indonesia BPOM Medical Device Registration

FX 80 Classix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320674. The device is manufactured by FRESENIUS MEDICAL CARE JAPAN K.K. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS MEDICAL CARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
FX 80 Classix
Analysis ID: AKL 20805320674

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FRESENIUS MEDICAL CARE INDONESIA

AR Address

Tempo Scan Tower Lt.20 JL. HR Rasuna Said Kav 3-4, Kuningan , Jakarta Selatan

Registration Date

Apr 10, 2023

Expiry Date

Feb 04, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Radiation Electromedics

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