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SEIMITSU CRP-F - Indonesia BPOM Medical Device Registration

SEIMITSU CRP-F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305024917. The device is manufactured by A CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEIMITSU DIAGNOSTICS.

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BPOM Registered
Risk Class Kelas Resiko : B
SEIMITSU CRP-F
Analysis ID: AKL 20305024917

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

A CO., LTD.

Country of Origin

Japan

Authorized Representative

PT. SEIMITSU DIAGNOSTICS

AR Address

Harton Tower 7th Floor, Jl. Boulevard Artha Gading, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara.

Registration Date

Sep 03, 2024

Expiry Date

Jul 26, 2026

Product Type

Immunological Test System

C-reactive protein immunological test system.

Invitro Diagnostics

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