USTAR II Surgical Instrument Non Steril - Indonesia BPOM Medical Device Registration
USTAR II Surgical Instrument Non Steril is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320456. The device is manufactured by UNITED ORTHOPEDIC CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOTECH INTI KORPORINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
UNITED ORTHOPEDIC CORPORATIONCountry of Origin
Taiwan (China)
Authorized Representative
PT. BIOTECH INTI KORPORINDOAR Address
Komplek Duta Merlin Blok D No. 11-13 Jalan Gajah Mada no 3-5 Lt. 2
Registration Date
Jul 19, 2023
Expiry Date
Aug 23, 2027
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
USTAR II Surgical Instrument Non Steril 2
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UNITED ORTHOPEDIC Surgical Instrument Non Steril
UNITED ORTHOPEDIC CORPORATION.
USTAR II Surgical Instrument Non Steril 2
UNITED ORTHOPEDIC CORPORATION
UNITED Hip System GTF II Stem
UNITED ORTHOPEDIC CORPORATION
UNITED ORTHOPEDIC Surgical Instrument Non Steril 2
UNITED ORTHOPEDIC CORPORATION.
UNITED U2 Knee System
UNITED ORTHOPEDIC CORPORATION
UNITED UCP Stem Cemented
UNITED ORTHOPEDIC CORPORATION
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UNITED ORTHOPEDIC CORPORATION
UNITED U2 Knee System 2
UNITED ORTHOPEDIC CORPORATION