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DIRUI BF - WNL Lyse - Indonesia BPOM Medical Device Registration

DIRUI BF - WNL Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220007. The device is manufactured by DIRUI INDUSTRIAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FAITHFUL MEDICAL GRACE.

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BPOM Registered
Risk Class Kelas Resiko : B
DIRUI BF - WNL Lyse
Analysis ID: AKL 20208220007

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Jul 09, 2022

Expiry Date

Jun 14, 2025

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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