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ADVIA Centaur CA 19-9 Diluent - Indonesia BPOM Medical Device Registration

ADVIA Centaur CA 19-9 Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208026078. 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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BPOM Registered
Risk Class Kelas Resiko : B
ADVIA Centaur CA 19-9 Diluent
Analysis ID: AKL 20208026078

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, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta

Registration Date

Oct 12, 2020

Expiry Date

Mar 04, 2025

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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