SERENITY Reflex Hammer - Indonesia BPOM Medical Device Registration
SERENITY Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001320147. The device is manufactured by ZHEJIANG HONSUN MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZHEJIANG HONSUN MEDICAL 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 07, 2023
Expiry Date
Feb 07, 2028
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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