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FAZZINI Reanimation Silicon Bag Child - Indonesia BPOM Medical Device Registration

FAZZINI Reanimation Silicon Bag Child is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403900145. The device is manufactured by FAZZINI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GEBANG SURYA HARAPAN.

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BPOM Registered
Risk Class Kelas Resiko : B
FAZZINI Reanimation Silicon Bag Child
Analysis ID: AKL 20403900145

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FAZZINI S.R.L.

Country of Origin

Italy

Authorized Representative

PT. GEBANG SURYA HARAPAN

AR Address

Ruko Puri Botanical Junction Blok I 10 No. 1 Jl. Raya Joglo RT 007 RW 001 Kel. Joglo, Kec. Kembangan, Jakarta Barat

Registration Date

Dec 19, 2022

Expiry Date

Mar 22, 2027

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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