SWANTIA Otoscope - Indonesia BPOM Medical Device Registration
SWANTIA Otoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703025322. The device is manufactured by SWANTIA MEDICAL (PVT) LIMITED from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRINITY ALPHA OMEGA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SWANTIA MEDICAL (PVT) LIMITEDCountry of Origin
Pakistan
Authorized Representative
PT. TRINITY ALPHA OMEGAAR Address
JL. Tanjung Duren Timur V No. 49 Jakarta Barat 11470
Registration Date
Sep 14, 2020
Expiry Date
Sep 14, 2025
Product Type
Ear, Nose and Throat Surgical Equipment
Otoscope.
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