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'PURIBLOOD" Leukocyte reduction filter for red blood cells - Indonesia BPOM Medical Device Registration

'PURIBLOOD" Leukocyte reduction filter for red blood cells is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209028127. The device is manufactured by INNOVATIVE MEDICAL MANUFACTURING COMPANY from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.

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Risk Class Kelas Resiko : C
'PURIBLOOD" Leukocyte reduction filter for red blood cells

โ€œPURIBLOODโ€ Leukocyte reduction filter for red blood cells

Analysis ID: AKL 20209028127

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Dec 22, 2020

Expiry Date

Oct 30, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Empty container for the collection and processing of blood and blood components.

Non Electromedic Sterile

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DJ Fang

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