CELLBOOSTER Lift - Indonesia BPOM Medical Device Registration
CELLBOOSTER Lift is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320296. The device is manufactured by SUISSELLE SA. from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SUISSELLE SA.Country of Origin
Switzerland
Authorized Representative
PT. SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530
Registration Date
Oct 26, 2023
Expiry Date
May 21, 2028
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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