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AGAPPE LX3 Bright - Indonesia BPOM Medical Device Registration

AGAPPE LX3 Bright is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220146. The device is manufactured by AGAPPE DIAGNOSTICS LTD from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIA CREATE HARMONY.

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
AGAPPE LX3 Bright

AGAPPE LX3 Lyse

Analysis ID: AKL 20208220146

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. PHILIA CREATE HARMONY

AR Address

PHILIA CIPTA HARMONI

Registration Date

Jul 08, 2022

Expiry Date

May 19, 2027

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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