BECKMAN COULTER Access CMV lgG - Indonesia BPOM Medical Device Registration
BECKMAN COULTER Access CMV lgG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220364. The device is manufactured by BIO - RAD ,INC from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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
BIO - RAD ,INCCountry of Origin
France
Authorized Representative
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
Jun 17, 2022
Expiry Date
Feb 10, 2026
Product Type
Serological Reagents
Cytomegalovirus serological reagents.
Invitro Diagnostics
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BECKMAN COULTER Access CMV lgG Calibrator
BECKMAN COULTER Access CMV lgG QC
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BECKMAN COULTER Access CEA Calibrator
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