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SYSMEX Lysercell WDF II - Indonesia BPOM Medical Device Registration

SYSMEX Lysercell WDF II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420067. The device is manufactured by SYSMEX CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is Sysmex Indonesia.

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BPOM Registered
Risk Class Kelas Resiko : B
SYSMEX Lysercell WDF II
Analysis ID: AKL 20208420067

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SYSMEX CORPORATION

Country of Origin

Japan

Authorized Representative

Sysmex Indonesia

AR Address

Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13

Registration Date

Apr 16, 2024

Expiry Date

Dec 07, 2028

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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