IVOCLAR VIVADENT OptraStick® - Indonesia BPOM Medical Device Registration
IVOCLAR VIVADENT OptraStick® is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602811284. The device is manufactured by IVOCLAR VIVADENT AG from Liechtenstein, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
IVOCLAR VIVADENT AGCountry 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
Sep 25, 2021
Expiry Date
Jul 31, 2026
Product Type
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