VIVAGLASS® CEM PL - Indonesia BPOM Medical Device Registration
VIVAGLASS® CEM PL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602811684. 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 MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IVOCLAR VIVADENT AG.Country of Origin
Liechtenstein
Authorized Representative
MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Sep 03, 2021
Expiry Date
Jul 31, 2026
Product Type
Prosthetic Dental Equipment
Dental cement.
Non Electromedic Non Sterile
IPS Empress® Direct
IPS E.MAX® Ceram
TETRIC® N-Flow 2
IPS IVOCOLOR
IPS E.MAX® Press
N-ETCH Etching Gel
VARIOLINK® N
TETRIC N-Flow
MONOBOND N
MULTILINK N
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