Stimuplex HNS 12 - Indonesia BPOM Medical Device Registration
Stimuplex HNS 12 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402220048. The device is manufactured by STOCKERT GMBH, GERMANY from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STOCKERT GMBH, GERMANYCountry of Origin
Germany
Authorized Representative
PT. B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Feb 21, 2023
Expiry Date
Feb 14, 2027
Product Type
Monitoring Anesthesia Equipment
Electrical peripheral nerve stimulator.
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