LIFECODES LSA™ Class I Kit - Indonesia BPOM Medical Device Registration
LIFECODES LSA™ Class I Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305918832. The device is manufactured by IMMUCOR GTI DIAGNOSTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IMMUCOR GTI DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Jan 17, 2020
Expiry Date
Dec 31, 2023
Product Type
Immunological Test System
Human leucocyte antibody
Invitro Diagnostics
STREPTAVIDIN-PE
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