IPS Empress® Direct - Indonesia BPOM Medical Device Registration
IPS Empress® Direct is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602811487. 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 PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IVOCLAR VIVADENT AG.Country of Origin
Liechtenstein
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
Jan 17, 2025
Expiry Date
Jul 31, 2026
Product Type
Prosthetic Dental Equipment
Tooth shade resin material.
Non Electromedic Non Sterile
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