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SEIMITSU Multi Control L-1 - Indonesia BPOM Medical Device Registration

SEIMITSU Multi Control L-1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324084. 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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Risk Class Kelas Resiko : B
SEIMITSU Multi Control L-1

SEIMITSU Multi Control L-1

Analysis ID: AKL 20101324084

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

A., CO., LTD

Country of Origin

Japan

Authorized Representative

PT. SEIMITSU DIAGNOSTICS

AR Address

MAYAPADA TOWER LANTAI 11 JL. JEND. SUDIRMAN KAV.28

Registration Date

Oct 11, 2023

Expiry Date

Oct 10, 2026

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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