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Atellica HEMA Diff - Indonesia BPOM Medical Device Registration

Atellica HEMA Diff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220159. 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 SIEMENS HEALTHINEERS 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
Atellica HEMA Diff
Analysis ID: AKL 20208220159

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HORIBA ABX SAS

Country of Origin

France

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta

Registration Date

Aug 15, 2022

Expiry Date

Mar 04, 2025

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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