AIM-V Medium - Indonesia BPOM Medical Device Registration
AIM-V Medium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302320331. The device is manufactured by LIFE TECHNOLOGIES CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OXFORD IMUNOTEK INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LIFE TECHNOLOGIES CORPORATIONCountry of Origin
United States
Authorized Representative
PT. OXFORD IMUNOTEK INDONESIAAR Address
Mixed Home Savoy B1-36, Jalan Perumahan Jakarta Garden City Boulevard RT 001 RW 006
Registration Date
Jul 17, 2023
Expiry Date
Nov 01, 2027
Product Type
Microbiology Equipment
Selective culture medium.
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