RESOUND ITE Hearing Aid - Indonesia BPOM Medical Device Registration
RESOUND ITE Hearing Aid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702320120. The device is manufactured by GN RESOUND A/S from Denmark, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PERSIFY MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GN RESOUND A/SCountry of Origin
Denmark
Authorized Representative
PT. PERSIFY MEDIKA INDONESIAAR Address
Jl. HR Rasuna Said Suite #B308 Lantai 3, Epicentrum Walk Office Suites, Kel. Karet Kuningan, Kec. Setiabudi, Kota Adm. Jakarta Selatan, DKI Jakarta
Registration Date
Jan 18, 2024
Expiry Date
Nov 30, 2025
Product Type
Prosthetic Ear, Nose and Throat Equipment
(Deleted) Hearing Aid.
Non Radiation Electromedics
