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BM DIAGNOSTICS BM Lyse - Indonesia BPOM Medical Device Registration

BM DIAGNOSTICS BM Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420239. The device is manufactured by DIRUI INDUSTRIAL CO., LTD., P.R. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUANA MITRA SUKSES.

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BPOM Registered
Risk Class Kelas Resiko : B
BM DIAGNOSTICS BM Lyse
Analysis ID: AKL 20208420239

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BUANA MITRA SUKSES

AR Address

RUKO NIAGA KALIMAS I BLOK B 10-11 JL INSPEKSI KALIMALANG

Registration Date

Sep 10, 2024

Expiry Date

May 01, 2027

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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