SWANTIA Percussion/Reflex Hammer - Indonesia BPOM Medical Device Registration
SWANTIA Percussion/Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001816478. 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.) LIMITED.Country of Origin
Pakistan
Authorized Representative
PT. TRINITY ALPHA OMEGAAR Address
JL. Tanjung Duren Timur V No. 49 Jakarta Barat 11470
Registration Date
May 01, 2021
Expiry Date
Dec 01, 2025
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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