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EAGLE CARE Diluent Solution - Indonesia BPOM Medical Device Registration

EAGLE CARE Diluent Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208813575. 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
EAGLE CARE Diluent Solution
Analysis ID: AKL 20208813575

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INAHO JAYA LESTARI

AR Address

Jl. Tentara Pelajar No. 42 - 42A

Registration Date

Mar 19, 2021

Expiry Date

Mar 19, 2024

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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