CRISTAL PRO - Indonesia BPOM Medical Device Registration
CRISTAL PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603023849. The device is manufactured by DELEO S.A.S from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DELEO S.A.SCountry of Origin
France
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan
Registration Date
Dec 02, 2024
Expiry Date
Nov 15, 2027
Product Type
Surgical Equipment
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