HAPPYPAPA ORIGINAL VERSION - Indonesia BPOM Medical Device Registration
HAPPYPAPA ORIGINAL VERSION is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21104420309. The device is manufactured by HEBEI YUCOS RUBBER TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CENTRAL HEALTHCARE UNGGUL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HEBEI YUCOS RUBBER TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. CENTRAL HEALTHCARE UNGGULAR Address
Mall Taman Palem Lantai 2 Blok A53 Jl. Kamal Raya No.13
Registration Date
Oct 14, 2024
Expiry Date
Oct 13, 2027
Product Type
Therapeutic Obstetric and Gynecological Equipment
Condom.
Non Electromedic Non Sterile
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