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PL1 Plasma Exchange Set - Indonesia BPOM Medical Device Registration

PL1 Plasma Exchange Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320556. The device is manufactured by FRESENIUS HEMOCARE NETHERLANDS B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FRESENIUS KABI INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
PL1 Plasma Exchange Set
Analysis ID: AKL 20209320556

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Netherlands

Authorized Representative

FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870

Registration Date

Jul 24, 2023

Expiry Date

Feb 21, 2028

Product Type

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

Automated blood cell separator

Non Electromedic Sterile

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