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ADVIA Centaur Multi Diluent 10 ReadyPack - Indonesia BPOM Medical Device Registration

ADVIA Centaur Multi Diluent 10 ReadyPack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208025951. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. (EAST WALPOLE) from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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Risk Class Kelas Resiko : B
ADVIA Centaur Multi Diluent 10 ReadyPack
Analysis ID: AKL 20208025951

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Registration Date

Feb 01, 2025

Expiry Date

Aug 01, 2029

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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