SWANTIA Laryngoscope - Indonesia BPOM Medical Device Registration
SWANTIA Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403420172. 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 TRINITY ALPHA OMEGA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SWANTIA MEDICAL (PVT) LIMITEDCountry of Origin
Pakistan
Authorized Representative
TRINITY ALPHA OMEGAAR Address
JL. Tanjung Duren Timur V No. 49 Jakarta Barat 11470
Registration Date
Mar 06, 2024
Expiry Date
Dec 05, 2026
Product Type
Therapeutic Anesthesia Equipment
Rigid laryngoscope.
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