ZISHEL Rose Mild - Indonesia BPOM Medical Device Registration
ZISHEL Rose Mild is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602917595. The device is manufactured by CHA MEDITECH CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
CHA MEDITECH CO., LTDCountry of Origin
Korea
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460
Registration Date
Jul 11, 2024
Expiry Date
May 10, 2029
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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