N Line - Indonesia BPOM Medical Device Registration
N Line is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420791. The device is manufactured by MEDLIGHT, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AESENDIA INFINI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDLIGHT, GMBHCountry of Origin
Germany
Authorized Representative
AESENDIA INFINI INDONESIAAR Address
Business Park Kebon Jeruk Blok D2 No. 10, Jl. Meruya Ilir Raya No. 88, Kode Pos 11620
Registration Date
Apr 05, 2024
Expiry Date
Oct 19, 2025
Product Type
Surgical Equipment
Ultraviolet lamp for dermatologic disorders.
Non Radiation Electromedics

