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CITO Infusion Set for Single Use - Indonesia BPOM Medical Device Registration

CITO Infusion Set for Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221401. The device is manufactured by WENZHOU K.L.F. MEDICAL PLASTICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FORDIC JAYA AWARD.

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BPOM Registered
Risk Class Kelas Resiko : C
CITO Infusion Set for Single Use
Analysis ID: AKL 20902221401

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FORDIC JAYA AWARD

AR Address

Ruko M Square Blok E No. 8 Jl. Cibaduyut Raya

Registration Date

Dec 12, 2022

Expiry Date

Dec 12, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Non Sterile

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