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EAGLECARE Uric Acid (UA) - Indonesia BPOM Medical Device Registration

EAGLECARE Uric Acid (UA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101026481. The device is manufactured by GENRUI BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INAHO JAYA LESTARI.

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
EAGLECARE Uric Acid (UA)
Analysis ID: AKL 20101026481

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GENRUI BIOTECH INC

Country of Origin

China

Authorized Representative

PT. INAHO JAYA LESTARI

AR Address

Jl. Tentara Pelajar No. 42 - 42A

Registration Date

Apr 07, 2021

Expiry Date

Apr 07, 2024

Product Type

Clinical Chemistry Test System

Uric acid test system (kit & cair)

Invitro Diagnostics

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