USTAR II Knee System - Indonesia BPOM Medical Device Registration
USTAR II Knee System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320735. The device is manufactured by UNITED ORTHOPEDIC CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BIOTECH INTI KORPORINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
UNITED ORTHOPEDIC CORPORATIONCountry of Origin
Taiwan (China)
Authorized Representative
BIOTECH INTI KORPORINDOAR Address
Komplek Duta Merlin Blok D No. 11-13 Jalan Gajah Mada no 3-5 Lt. 2
Registration Date
Jun 20, 2023
Expiry Date
Aug 23, 2027
Product Type
Prosthetic Orthopedic Equipment
Knee joint femorotibial metal/polymer constrained cemented prosthesis.
Non Electromedic Sterile
USTAR II Surgical Instrument Non Steril 2
USTAR II Surgical Instrument Non Steril
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