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DJMED Finger Pulse Oximeter - Indonesia BPOM Medical Device Registration

DJMED Finger Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502124816. The device is manufactured by SHENZHEN FITFAITH TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WITH JAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
DJMED Finger Pulse Oximeter
Analysis ID: AKL 20502124816

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. WITH JAYA MEDIKA

AR Address

Desa Tinom Sidoarum

Registration Date

Aug 06, 2021

Expiry Date

Aug 05, 2024

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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