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DIRUI BF-FDO IN Lyse - Indonesia BPOM Medical Device Registration

DIRUI BF-FDO IN Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208022370. 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 PT. FAITHFUL MEDICAL GRACE.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
DIRUI BF-FDO IN Lyse

DIRUI BF-FDO I Lyse

Analysis ID: AKL 20208022370

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

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

Registration Date

Nov 03, 2023

Expiry Date

Jun 30, 2028

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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