PRIMAMED SCHWERT Neurology Instrument, Percussion Hammer - Indonesia BPOM Medical Device Registration
PRIMAMED SCHWERT Neurology Instrument, Percussion Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001611802. The device is manufactured by A. SCHWEICKHARDT GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA PRIMA MANDIRI JAYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
A. SCHWEICKHARDT GMBH & CO., KG.Country of Origin
Germany
Authorized Representative
PT. DAYA PRIMA MANDIRI JAYAAR Address
JL. KALIGARANG 1A SEMARANG
Registration Date
Nov 23, 2023
Expiry Date
Nov 22, 2026
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile
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