Pure Global

PRIMELINE Lyse Reagent 3-Diff - Indonesia BPOM Medical Device Registration

PRIMELINE Lyse Reagent 3-Diff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320445. The device is manufactured by AEHEALTH LIMITED from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTI SARANA MEDIKA.

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
PRIMELINE Lyse Reagent 3-Diff
Analysis ID: AKL 20208320445

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AEHEALTH LIMITED

Country of Origin

China

Authorized Representative

PT. MULTI SARANA MEDIKA

AR Address

Komp. Gading Bukit Indah Jl. Bukit Gading Raya Blok B Kav. No.1

Registration Date

Feb 21, 2023

Expiry Date

Feb 20, 2026

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