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TERUMO Automatic Component Extractor T-ACE II+ and - Indonesia BPOM Medical Device Registration

TERUMO Automatic Component Extractor T-ACE II+ and is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209111412. The device is manufactured by TERUMO BCT EUROPE N.V. from Belgium, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
TERUMO Automatic Component Extractor T-ACE II+ and
Analysis ID: AKL 20209111412

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Belgium

Authorized Representative

PT. TERUMO INDONESIA

AR Address

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

Registration Date

Dec 16, 2020

Expiry Date

Nov 17, 2025

Product Type

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

Automated blood cell separator

Invitro Diagnostics

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