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TRIMA ACCEL Multiplasma Set - Indonesia BPOM Medical Device Registration

TRIMA ACCEL Multiplasma Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209310696. The device is manufactured by TERUMO BCT. INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TERUMO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
TRIMA ACCEL Multiplasma Set
Analysis ID: AKL 20209310696

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TERUMO BCT. INC.

Country of Origin

United States

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Mar 24, 2022

Expiry Date

Mar 09, 2027

Product Type

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

Transfer set.

Non Electromedic Sterile

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