BECKMAN COULTER Access Progesterone II - Indonesia BPOM Medical Device Registration
BECKMAN COULTER Access Progesterone II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520128. The device is manufactured by BECKMAN COULTER ,INC from United States, 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 ,INCCountry of Origin
United States
Authorized Representative
PT. DHH TRADING INDONESIAAR Address
Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan
Registration Date
Jan 20, 2025
Expiry Date
Mar 28, 2029
Product Type
Clinical Chemistry Test System
Progesterone test system (kit & cair)
Invitro Diagnostics
BECKMAN COULTER Access Thyroglobulin Antibody - II
BECKMAN COULTER ,INC
BECKMAN COULTER Access Thyroglobulin
BECKMAN COULTER, INC (CHASKA)
iQ Precision Kit
BECKMAN COULTER INC.
iQ Body Fluids Lysing Reagent
BECKMAN COULTER INC.
iChem VELOCITY Urine Chemistry Strips
BECKMAN COULTER IRELAND, INC.
iQ 200 Sprint Plus Analyzer (2008 Version) (Int'l)
BECKMAN COULTER INC.
iChemยฎ VELOCITYโข CalChek Kit
BECKMAN COULTER, INC.
iQ Control/Focus Set
BECKMAN COULTER INC.
iQ Laminaโข
BECKMAN COULTER, INC.
iQ Lamina
BECKMAN COULTER GMBH

