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WITLEAF Handheld Pulse Oximeter S300 - Indonesia BPOM Medical Device Registration

WITLEAF Handheld Pulse Oximeter S300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502129220. The device is manufactured by SHENZHEN WITLEAF MEDICAL ELECTRONICS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDONESIAN MEDICAL INNOVATION.

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BPOM Registered
Risk Class Kelas Resiko : B
WITLEAF Handheld Pulse Oximeter S300
Analysis ID: AKL 20502129220

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDONESIAN MEDICAL INNOVATION

AR Address

Taman Buaran Indah I, Blok W/400

Registration Date

Dec 31, 2021

Expiry Date

Dec 31, 2023

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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