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YHLO iFlash LH - Indonesia BPOM Medical Device Registration

YHLO iFlash LH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124603. The device is manufactured by SHENZHEN YHLO BIOTECH CO,,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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
YHLO iFlash LH
Analysis ID: AKL 20101124603

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Jul 29, 2021

Expiry Date

Feb 04, 2026

Product Type

Clinical Chemistry Test System

Luteinizing hormone test system (kit & cair)

Invitro Diagnostics

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