HELIOSIT® Orthodontic - Indonesia BPOM Medical Device Registration
HELIOSIT® Orthodontic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602026488. The device is manufactured by IVOCLAR VIVADENT AG. from Liechtenstein, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IVOCLAR VIVADENT AG.Country of Origin
Liechtenstein
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Oct 03, 2022
Expiry Date
Jul 31, 2026
Product Type
Prosthetic Dental Equipment
Bracket adhesive resin and tooth conditioner.
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