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ABX Diluent - Indonesia BPOM Medical Device Registration

ABX Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208810558. The device is manufactured by HORIBA ABX SAS. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HORIBA INDONESIA.

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
ABX Diluent
Analysis ID: AKL 20208810558

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HORIBA ABX SAS.

Country of Origin

France

Authorized Representative

PT. HORIBA INDONESIA

AR Address

Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang

Registration Date

Mar 07, 2023

Expiry Date

Oct 01, 2027

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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