IPS e.max® ZirCAD LT - Indonesia BPOM Medical Device Registration
IPS e.max® ZirCAD LT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605126255. The device is manufactured by IVOCLAR VIVADENT MANUFACTURING 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
IVOCLAR VIVADENT MANUFACTURING 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
Apr 02, 2024
Expiry Date
Jul 31, 2026
Product Type
Other Dental Equipment
Porcelain powder for clinical use.
Non Electromedic Non Sterile
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