SERENITY Tens & Muscle Stimulator - Indonesia BPOM Medical Device Registration
SERENITY Tens & Muscle Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003420093. The device is manufactured by SHENZHEN ASTEC TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN ASTEC TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
Sep 23, 2024
Expiry Date
Feb 07, 2028
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
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