QUIKLYTE Integrated Multisensor Flush Solution - Indonesia BPOM Medical Device Registration
QUIKLYTE Integrated Multisensor Flush Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204122335. The device is manufactured by NOVA BIOMEDICAL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
NOVA BIOMEDICAL CORPORATIONCountry of Origin
United States
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Feb 05, 2025
Expiry Date
Aug 01, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
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