UNITEK Prestige Series Hand Instrument - Indonesia BPOM Medical Device Registration
UNITEK Prestige Series Hand Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603716797. The device is manufactured by HU-FRIEDY MFG. CO., LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 3M INDONESIA IMPORTAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HU-FRIEDY MFG. CO., LLC.Country of Origin
United States
Authorized Representative
3M INDONESIA IMPORTAMAAR Address
KAWASAN PERKANTORAN HIJAU ARKADIA, TOWER F, LT.9, JL. TB. SIMATUPANG KAV. 88
Registration Date
Jan 27, 2022
Expiry Date
Dec 19, 2024
Product Type
Surgical Dental Equipment
Dental hand instrument.
Non Electromedic Non Sterile
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