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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BECKMAN COULTER IRELAND,INC.Country of Origin
Ireland
Authorized Representative
PT. DHH TRADING INDONESIAAR 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)
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