Sagemax NexxZr® S - Indonesia BPOM Medical Device Registration
Sagemax NexxZr® S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605025045. The device is manufactured by SAGEMAX BIOCERAMICS, INC. from United States, 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
SAGEMAX BIOCERAMICS, INC.Country of Origin
United States
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Jun 28, 2022
Expiry Date
May 14, 2024
Product Type
Other Dental Equipment
Porcelain powder for clinical use.
Non Electromedic Non Sterile
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