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BECKMAN COULTER ISE Internal Reference - Indonesia BPOM Medical Device Registration

BECKMAN COULTER ISE Internal Reference is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221557. The device is manufactured by BECKMAN COULTER IRELAND INC. from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING INDONESIA.

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Risk Class Kelas Resiko : B
BECKMAN COULTER ISE Internal Reference
Analysis ID: AKL 20101221557

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. DHH TRADING INDONESIA

AR Address

Gedung World Trade Center 3, Lt. 20, Jl. Jend. Sudirman Kav. 29-31, Kel. Karet, Kec. Setiabudi, Jakarta Selatan, DKI Jakarta

Registration Date

Sep 26, 2022

Expiry Date

Feb 10, 2026

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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