SepaSperm - Indonesia BPOM Medical Device Registration
SepaSperm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105320063. The device is manufactured by KITAZATO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SONNA MEDIKA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KITAZATO CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. SONNA MEDIKA JAYAAR Address
Rukan Sentra Niaga Blok M, Green Lake City, No.017 RT. 007 RW.008, Duri Kosambi, Cengkareng, Jakarta Barat
Registration Date
Jun 11, 2023
Expiry Date
Jul 17, 2026
Product Type
Reproductive Aids
Reproductive media and supplements.
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