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FX CORDIAX 80 - Indonesia BPOM Medical Device Registration

FX CORDIAX 80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805916880. The device is manufactured by FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH from Germany, 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 CORDIAX 80
Analysis ID: AKL 20805916880

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

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 22, 2024

Expiry Date

Dec 05, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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