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DEWEI Lyse-DW3680 - Indonesia BPOM Medical Device Registration

DEWEI Lyse-DW3680 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208917516. The device is manufactured by DEWEI MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISTA MAIN.

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
DEWEI Lyse-DW3680
Analysis ID: AKL 20208917516

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDISTA MAIN

AR Address

Jl. Pondok Cibubur No. 133

Registration Date

Dec 17, 2023

Expiry Date

Nov 01, 2027

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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