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Nesco Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

Nesco Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420075. 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. DJUNIAR & DJUNIAR.

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BPOM Registered
Risk Class Kelas Resiko : B
Nesco Handheld Pulse Oximeter
Analysis ID: AKL 20502420075

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420

Registration Date

Feb 19, 2024

Expiry Date

Nov 27, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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