ACUMED Fibula Nail 2 System Instrument - Indonesia BPOM Medical Device Registration
ACUMED Fibula Nail 2 System Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320461. The device is manufactured by ACUMED LLC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PRO-HEALTH INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ACUMED LLCCountry of Origin
United States
Authorized Representative
PRO-HEALTH INTERNATIONALAR Address
Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5
Registration Date
Jul 28, 2023
Expiry Date
Jan 12, 2027
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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