ACUMED Polarus 3 Solution System Instruments - Indonesia BPOM Medical Device Registration
ACUMED Polarus 3 Solution System Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420421. 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 PT. PRO-HEALTH INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ACUMED LLCCountry of Origin
United States
Authorized Representative
PT. PRO-HEALTH INTERNATIONALAR Address
Komplek Perkantoran Duta Merlin Blok C 35-36, Jl. Gajah Mada 3-5 RT 002 RW 005, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Gambir, Kel. Petojo Utara
Registration Date
Dec 17, 2024
Expiry Date
Jan 12, 2027
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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