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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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BPOM Registered
Risk Class Kelas Resiko : A
GENESIS ™ Tube Sealer SE-330
Analysis ID: AKL 10209610369

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. PRIMA ALKESINDO NUSANTARA

AR 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.

Invitro Diagnostics

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