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FISHER & PAYKEL Vented Autofeed Humidification Chamber - Indonesia BPOM Medical Device Registration

FISHER & PAYKEL Vented Autofeed Humidification Chamber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403718803. The device is manufactured by FISHER & PAYKEL HEALTHCARE SA DE CV. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.

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BPOM Registered
Risk Class Kelas Resiko : B
FISHER & PAYKEL Vented Autofeed Humidification Chamber
Analysis ID: AKL 20403718803

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. MURSMEDIC

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

Nov 24, 2022

Expiry Date

May 19, 2025

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Electromedic Non Sterile

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