KOEL TRINITY - Indonesia BPOM Medical Device Registration
KOEL TRINITY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321393. The device is manufactured by KOELIS from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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KOELIS TRINITY
Risk Classification
Product Class
Kelas : 2
Manufacturer
KOELISCountry of Origin
France
Authorized Representative
TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Nov 21, 2023
Expiry Date
Apr 21, 2028
Product Type
Diagnostic Radiology Equipment
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