ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls - Indonesia BPOM Medical Device Registration

ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220041. The device is manufactured by DASH INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls

Analysis ID: AKL 20208220041

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DASH INC.

Country of Origin

United States

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

Feb 25, 2022

Expiry Date

Mar 04, 2025

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

DJ Fang

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Other Products from DASH INC.

Products from the same manufacturer (10 products)

ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

iQ Body Fluids Controls-Level I and Level II

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