SAGEMAX NexxZr T (1) - Indonesia BPOM Medical Device Registration
SAGEMAX NexxZr T (1) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605025086. 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
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
May 29, 2024
Expiry Date
Apr 25, 2029
Product Type
Other Dental Equipment
Porcelain powder for clinical use.
Non Electromedic Non Sterile
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