IMUGARD III-PL - Indonesia BPOM Medical Device Registration
IMUGARD III-PL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902412323. The device is manufactured by FUJINOMIYA FACTORY OF TERUMO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJINOMIYA FACTORY OF TERUMO CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
May 27, 2019
Expiry Date
Mar 06, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set.
Non Electromedic Sterile
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