HP Cell Vitaran I - Indonesia BPOM Medical Device Registration
HP Cell Vitaran I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320284. The device is manufactured by BR PHARM CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SMELL MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BR PHARM CO., LTDCountry of Origin
Korea
Authorized Representative
SMELL MEDICAL INDONESIAAR Address
Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta
Registration Date
Oct 04, 2023
Expiry Date
Jul 20, 2028
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
STICOL Soft
PRP SCIENCE CO., LTD.
JUVELOOK
SPIRIT CO., LTD
MEGAGEN Accessory (2)
MEGAGEN IMPLANT CO., LTD.
HP Vitaran
BR PHARM CO., LTD
MEGAGEN AnyRidge Internal Fixture
MEGAGEN IMPLANT CO., LTD.
CUREJET
BAZ BIOMEDIC CO., LTD
AGNES
AGNES MEDICAL CO., LTD
B&E
B&E KOREA CO., LTD
VIVABELLA
SPIRIT CO., LTD
B&E
B&E KOREA CO., LTD

