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TERUFUSION Infusion Pump Type LM3 - Indonesia BPOM Medical Device Registration

TERUFUSION Infusion Pump Type LM3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902814325. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION JAPAN. from Japan, 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
TERUFUSION Infusion Pump Type LM3
Analysis ID: AKL 20902814325

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. TERUMO INDONESIA

AR Address

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

Registration Date

Apr 16, 2024

Expiry Date

Sep 15, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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