PROSTROLANE NATURAL_B - Indonesia BPOM Medical Device Registration
PROSTROLANE NATURAL_B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602917336. 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 HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
CAREGEN CO., LTDCountry of Origin
Korea
Authorized Representative
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
Sep 08, 2022
Expiry Date
Jul 07, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
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