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DIRUI BF-FBH LYSE - Indonesia BPOM Medical Device Registration

DIRUI BF-FBH LYSE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420278. 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 DIRUI MEDICAL INDONESIA.

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-FBH LYSE
Analysis ID: AKL 20208420278

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

DIRUI MEDICAL INDONESIA

AR Address

Kompleks Pergudangan Green Sedayu Bizpark Cakung, Blok GS 6 Nomor 26

Registration Date

Sep 24, 2024

Expiry Date

Dec 16, 2028

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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