MOTUS AY - Indonesia BPOM Medical Device Registration
MOTUS AY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323353. The device is manufactured by DEKA M.E.L.A S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEKA M.E.L.A S.R.L.Country of Origin
Italy
Authorized Representative
CEKINDO BUSINESS INTERNATIONALAR Address
CEKINDO BUSINESS INTERNATIONAL
Registration Date
Feb 20, 2023
Expiry Date
Nov 15, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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