GLOTECH Blood Centrifugal - Indonesia BPOM Medical Device Registration
GLOTECH Blood Centrifugal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209320554. The device is manufactured by HUNAN HEREXI INSTRUMENT & EQUIPMENT 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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GLOTECH Blood Centrifuge
Risk Classification
Product Class
Kelas : 1
Manufacturer
HUNAN HEREXI INSTRUMENT & EQUIPMENT CO.,LTDCountry of Origin
China
Authorized Representative
PT. GLOMED ADINATA PRIMAAR Address
Jl. Gunung Sahari Raya No.2 Blok E/23-A Kelurahan : Pademangan Barat Kecamatan : Pademangan
Registration Date
Jul 21, 2023
Expiry Date
Nov 10, 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.
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