RZ Kerrison Instrument Set I - Indonesia BPOM Medical Device Registration
RZ Kerrison Instrument Set I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002420070. The device is manufactured by RZ MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RZ MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
PT. SIGMA KARSA MAGNAAR Address
Ruko Mega Grosir Cempaka Mas, Jl. Letjen Suprapto Blok J No. 37-38 RW.08, Kel. Sumur Batu, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Aug 19, 2024
Expiry Date
Dec 31, 2028
Product Type
Surgical Neurology Equipment
Nonpowered neurosurgical instrument.
Non Electromedic Non Sterile
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