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GLOTECH Hematocrit Centrifuge - Indonesia BPOM Medical Device Registration

GLOTECH Hematocrit Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209914867. The device is manufactured by ZENITH LAB (JIANGSU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOMED ADINATA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : A
GLOTECH Hematocrit Centrifuge
Analysis ID: AKL 10209914867

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GLOMED ADINATA PRIMA

AR Address

Jl. Gunung Sahari Raya No.2 Blok E/23-A Kelurahan : Pademangan Barat Kecamatan : Pademangan

Registration Date

Mar 21, 2022

Expiry Date

Mar 19, 2025

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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