Pure Global

AMS LYSE LD - Indonesia BPOM Medical Device Registration

AMS LYSE LD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220065. 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. TIRTA PASIFIK MEDIKATAMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
AMS LYSE LD
Analysis ID: AKL 20208220065

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TIRTA PASIFIK MEDIKATAMA

AR Address

TIRTA PASIFIK MEDIKATAMA

Registration Date

Mar 23, 2022

Expiry Date

Dec 31, 2024

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing