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Atellica IM Acid - Indonesia BPOM Medical Device Registration

Atellica IM Acid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320470. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. USA from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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 : A
Atellica IM Acid
Analysis ID: AKL 10204320470

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. 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

May 20, 2023

Expiry Date

Mar 04, 2025

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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