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MEDIANA BODY COMPOSITION ANALYZER I30 - Indonesia BPOM Medical Device Registration

MEDIANA BODY COMPOSITION ANALYZER I30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502120590. The device is manufactured by MEDIAN CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ASA PRATAMA PARTNERS.

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BPOM Registered
Risk Class Kelas Resiko : B
MEDIANA BODY COMPOSITION ANALYZER I30
Analysis ID: AKL 20502120590

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDIAN CO.,LTD

Country of Origin

Korea

Authorized Representative

ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

Jul 05, 2023

Expiry Date

Sep 01, 2026

Product Type

Monitoring Cardiology Equipment

Impedance plethysmograph.

Non Radiation Electromedics

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