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GINEVRI Neonatal Resuscitator - Indonesia BPOM Medical Device Registration

GINEVRI Neonatal Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403511834. The device is manufactured by GENEVA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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Risk Class Kelas Resiko : C
GINEVRI Neonatal Resuscitator
Analysis ID: AKL 20403511834

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

GENEVA S.R.L.

Country of Origin

Italy

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Mar 04, 2022

Expiry Date

Oct 25, 2026

Product Type

Therapeutic Anesthesia Equipment

Noncontinuous ventilator (IPPB).

Non Radiation Electromedics

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