KUBOTA Benchtop Centrifuge - Indonesia BPOM Medical Device Registration
KUBOTA Benchtop Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209915542. The device is manufactured by KUBOTA MANUFACTURING CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KUBOTA MANUFACTURING CORPORATIONCountry of Origin
Japan
Authorized Representative
DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Nov 19, 2021
Expiry Date
Aug 27, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood bank centrifuge for in vitro diagnostic use.
Invitro Diagnostics
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