CELLBOOSTER Glow - Indonesia BPOM Medical Device Registration
CELLBOOSTER Glow is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320255. The device is manufactured by SUISSELLE SA from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SUISSELLE SACountry of Origin
Switzerland
Authorized Representative
SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G, Jl. Panjang No. 5
Registration Date
Sep 07, 2023
Expiry Date
May 22, 2028
Product Type
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