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FISHER & PAYKEL MyAIRVO 2 Humidifier - Indonesia BPOM Medical Device Registration

FISHER & PAYKEL MyAIRVO 2 Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403818710. The device is manufactured by FISHER AND PAYKEL HEALTHCARE LTD. from New Zealand, 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 MyAIRVO 2 Humidifier
Analysis ID: AKL 20403818710

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

New Zealand

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 10, 2022

Expiry Date

May 19, 2025

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Radiation Electromedics

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