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ABX Pentra Reference 280 ml - Indonesia BPOM Medical Device Registration

ABX Pentra Reference 280 ml is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520327. The device is manufactured by HORIBA ABX SAS, FRANCE 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 Pentra Reference 280 ml
Analysis ID: AKL 20101520327

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Feb 08, 2025

Expiry Date

Oct 30, 2029

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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