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TRISMED Cardipia 400 H Electrocardiograph - Indonesia BPOM Medical Device Registration

TRISMED Cardipia 400 H Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502515382. The device is manufactured by TRISMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : B
TRISMED Cardipia 400 H Electrocardiograph
Analysis ID: AKL 20502515382

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TRISMED CO., LTD.

Country of Origin

Korea

Authorized Representative

PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Jan 04, 2024

Expiry Date

Feb 28, 2027

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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