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TRISMED CARDIPIA 800 H Electrocardiograph - Indonesia BPOM Medical Device Registration

TRISMED CARDIPIA 800 H Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502914276. 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 PT. PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : B
TRISMED CARDIPIA 800 H Electrocardiograph
Analysis ID: AKL 20502914276

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TRISMED CO, LTD.

Country of Origin

Korea

Authorized Representative

PT. PRIMARY WORKS

AR Address

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

Registration Date

Jan 25, 2023

Expiry Date

Dec 21, 2027

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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