CAVEX – ProphyPaste - Indonesia BPOM Medical Device Registration
CAVEX – ProphyPaste is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605420435. The device is manufactured by CAVEX HOLLAND B.V from Netherlands, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CAVEX HOLLAND B.VCountry of Origin
Netherlands
Authorized Representative
LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223
Registration Date
Oct 22, 2024
Expiry Date
Dec 31, 2027
Product Type
Other Dental Equipment
Oral cavity abrasive polishing agent.
Non Electromedic Non Sterile
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