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ADIAG Lyse LH - Indonesia BPOM Medical Device Registration

ADIAG Lyse LH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320543. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALIZAH.

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
ADIAG Lyse LH
Analysis ID: AKL 20208320543

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALIZAH

AR Address

JL. OTISTA III NO.10A RT 001 RW 004 KEL.CIPINANG CEMPEDAK KEC.JATINEGARA

Registration Date

May 04, 2023

Expiry Date

Apr 28, 2026

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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DJ Fang

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