SOLID - Reflex Hammer - Indonesia BPOM Medical Device Registration
SOLID - Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001020656. The device is manufactured by ZHANGJIAGANG SHUANGYIN MEDICAL INSTRUMENTS CO. LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ARITEK KARYA MANDIRI.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
ARITEK KARYA MANDIRIAR Address
Green Lake City Rukan Crown Blok. A No. 19 Kelurahan Petir, Kecamatan Cipondoh Tangerang, Banten
Registration Date
Jan 24, 2024
Expiry Date
Jan 15, 2029
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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