GEA Reflect Hammer - Indonesia BPOM Medical Device Registration
GEA Reflect Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001918440. The device is manufactured by HONSUN (NANTONG) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HONSUN (NANTONG) CO., LTD.Country of Origin
China
Authorized Representative
MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Sep 30, 2022
Expiry Date
Sep 29, 2025
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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