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KLARA Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

KLARA Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502915399. The device is manufactured by UTECH CO.LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARITEK KARYA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
KLARA Handheld Pulse Oximeter
Analysis ID: AKL 20502915399

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

UTECH CO.LTD.

Country of Origin

China

Authorized Representative

PT. ARITEK KARYA MANDIRI

AR Address

Green Lake City Rukan Crown Blok. A No. 19 Kelurahan Petir, Kecamatan Cipondoh Tangerang, Banten

Registration Date

Nov 14, 2023

Expiry Date

Dec 13, 2025

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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