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ALPHAMED Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

ALPHAMED Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502123235. The device is manufactured by UTECH.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ALPHAMED Handheld Pulse Oximeter
Analysis ID: AKL 20502123235

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

UTECH.,LTD

Country of Origin

China

Authorized Representative

PT. CIPTA MEDIKA INDONESIA

AR Address

GRAND UNEDO JL. BINA MARGA NO. 94 G

Registration Date

Jun 03, 2021

Expiry Date

Jun 02, 2024

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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