Q-US+ - Indonesia BPOM Medical Device Registration
Q-US+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602023741. The device is manufactured by OSSTEM IMPLANT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OSSTEM IMPLANT.
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Q-Oss+
Risk Classification
Product Class
Kelas : 2
Manufacturer
OSSTEM IMPLANT CO., LTD.Country of Origin
Korea
Authorized Representative
PT. OSSTEM IMPLANTAR Address
K-link Office Tower Lt. 27 Jl. Jend Gatot Subroto No 59 A
Registration Date
Mar 11, 2024
Expiry Date
Feb 07, 2029
Product Type
Prosthetic Dental Equipment
Bone grafting material.
Non Electromedic Sterile
OSSTEM Superstructure System (Abutment)-6
OSSTEM OssBuilder
OSSTEM MS Implant Provisional
OSSTEM Superstructure Protect Cap
OSSTEM Impression Material-HySil Plus
OSSTEM Impression Material HySil Super Fast
OSSTEM Bone Screw & Tenting Screw
OSSTEM Superstructure System (1)
OSSTEM Instrument System (1)
OSSTEM Driver System
OSSTEM Superstructure System (Abutment)-6
OSSTEM IMPLANT CO., LTD.
OSSTEM OssBuilder
OSSTEM IMPLANT CO., LTD.
OSSTEM Superstructure Protect Cap
OSSTEM IMPLANT CO., LTD.
OSSTEM MS Implant Provisional
OSSTEM IMPLANT CO., LTD.
OSSTEM Impression Material-HySil Plus
OSSTEM IMPLANT CO., LTD.
OSSTEM Impression Material HySil Super Fast
OSSTEM IMPLANT CO., LTD.
OSSTEM Bone Screw & Tenting Screw
OSSTEM IMPLANT CO., LTD.
OSSTEM Superstructure System (1)
OSSTEM IMPLANT CO., LTD.
OSSTEM Instrument System (1)
OSSTEM IMPLANT CO., LTD.
OSSTEM Driver System
OSSTEM IMPLANT CO., LTD.