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BECKMAN COULTER Creatinine - Indonesia BPOM Medical Device Registration

BECKMAN COULTER Creatinine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220511. 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.

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 : B
BECKMAN COULTER Creatinine
Analysis ID: AKL 20101220511

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. DHH TRADING INDONESIA

AR Address

Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan

Registration Date

Mar 15, 2024

Expiry Date

Feb 10, 2026

Product Type

Clinical Chemistry Test System

Creatine test system (kit & cair)

Invitro Diagnostics

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