GENESIS ™ Tube Sealer SE-330 - Indonesia BPOM Medical Device Registration
GENESIS ™ Tube Sealer SE-330 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209610369. The device is manufactured by CENTRON TECHNOLOGIES CORPORATION. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CENTRON TECHNOLOGIES CORPORATION.Country of Origin
Korea
Authorized Representative
PT. PRIMA ALKESINDO NUSANTARAAR Address
Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara
Registration Date
Jul 29, 2019
Expiry Date
Feb 13, 2024
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Heat-sealing device.
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