Pure Global

Luminex Sheath Fluid - 20 liters - Indonesia BPOM Medical Device Registration

Luminex Sheath Fluid - 20 liters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320444. The device is manufactured by LUMINEX CORP from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SETIA GUNA 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 : A
Luminex Sheath Fluid - 20 liters
Analysis ID: AKL 10204320444

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

LUMINEX CORP

Country of Origin

United States

Authorized Representative

SETIA GUNA MEDIKA

AR Address

KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT

Registration Date

Apr 28, 2023

Expiry Date

Dec 31, 2024

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from LUMINEX CORP
Products from the same manufacturer (2 products)