OSSTEM SM3 - Indonesia BPOM Medical Device Registration
OSSTEM SM3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603121443. The device is manufactured by NAKANISHI INC. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. OSSTEM IMPLANT.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NAKANISHI INC.Country of Origin
Japan
Authorized Representative
PT. OSSTEM IMPLANTAR Address
K-link Office Tower Lt. 27 Jl. Jend Gatot Subroto No 59 A
Registration Date
Mar 17, 2021
Expiry Date
Aug 31, 2025
Product Type
Surgical Dental Equipment
Dental handpiece and accessories
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OSSTEM Superstructure System (Abutment)-6
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OSSTEM OssBuilder
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OSSTEM Superstructure Protect Cap
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OSSTEM MS Implant Provisional
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OSSTEM Impression Material-HySil Plus
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OSSTEM Impression Material HySil Super Fast
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OSSTEM Bone Screw & Tenting Screw
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OSSTEM Superstructure System (1)
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OSSTEM Instrument System (1)
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OSSTEM Driver System
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