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BECKMAN COULTER LDH - Indonesia BPOM Medical Device Registration

BECKMAN COULTER LDH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322395. 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 LDH
Analysis ID: AKL 20101322395

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

Jan 25, 2023

Expiry Date

Feb 10, 2026

Product Type

Clinical Chemistry Test System

Lactate dehydrogenase test system (kit & cair)

Invitro Diagnostics

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