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MEDLUME GENFLOW Blood / Fluid Warmer - Indonesia BPOM Medical Device Registration

MEDLUME GENFLOW Blood / Fluid Warmer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209311128. The device is manufactured by HOTECH INSTRUMENT CORPORATION . from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMPM HEALTHCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
MEDLUME GENFLOW Blood / Fluid Warmer
Analysis ID: AKL 20209311128

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Sep 26, 2023

Expiry Date

Apr 21, 2028

Product Type

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

Blood and plasma warming device.

Non Radiation Electromedics

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