DKMP Vasculuminator - Indonesia BPOM Medical Device Registration
DKMP Vasculuminator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901411500. The device is manufactured by DKMS B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAGNIFICENT ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DKMS B.V.Country of Origin
Netherlands
Authorized Representative
PT. MAGNIFICENT ALKESINDOAR Address
Jl. Rawa Bambu Raya No. 15 F-H
Registration Date
Oct 21, 2021
Expiry Date
Oct 13, 2024
Product Type
General and Individual Hospital Equipment Monitoring
Electronic monitor for gravity flow infusion systems.
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