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AIRTECH Oxygen Regulator - Indonesia BPOM Medical Device Registration

AIRTECH Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220041. The device is manufactured by DANYANG AIRTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is LUMARY BIRUMAS.

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BPOM Registered
Risk Class Kelas Resiko : A
AIRTECH Oxygen Regulator
Analysis ID: AKL 10402220041

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

LUMARY BIRUMAS

AR Address

Gd. Menara Palma Lt. 12 Jl. H.R. Rasuna Said Blok X-2, Kav.6 Jakarta 12950

Registration Date

Jun 22, 2024

Expiry Date

May 15, 2029

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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