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ALARIS ™ Product. SmartSite ™ Needle-free System. TRANSFUSION/BOOD SET. VENTED. 200 µm FILTER. - Indonesia BPOM Medical Device Registration

ALARIS ™ Product. SmartSite ™ Needle-free System. TRANSFUSION/BOOD SET. VENTED. 200 µm FILTER. is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902120241. The device is manufactured by CAREFUSION BH 335 D.O.O. CAZIN from Bosnia And Herzegovina, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BECTON DICKINSON INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
ALARIS ™ Product. SmartSite ™ Needle-free System. TRANSFUSION/BOOD SET. VENTED. 200 µm FILTER.
Analysis ID: AKL 20902120241

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Bosnia And Herzegovina

Authorized Representative

BECTON DICKINSON INDONESIA

AR Address

Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46

Registration Date

Feb 06, 2025

Expiry Date

Jan 09, 2030

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

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