PROSTROLANE BLANC_B - Indonesia BPOM Medical Device Registration
PROSTROLANE BLANC_B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602914301. The device is manufactured by CAREGEN 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
CAREGEN CO., LTDCountry of Origin
Korea
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
TAMAN HARAPAN INDAH BLOK FF I-B NO.10 RT. 014 RW.007
Registration Date
Oct 01, 2024
Expiry Date
Jul 07, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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