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ALVITAL Fingertip Pulse Oximeter - Indonesia BPOM Medical Device Registration

ALVITAL Fingertip Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502120477. The device is manufactured by LEADTEK RESEARCH INC., from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ALVITAL Fingertip Pulse Oximeter
Analysis ID: AKL 20502120477

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. INNOVATION HEALTHCARE INDONESIA

AR Address

Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450

Registration Date

Sep 20, 2024

Expiry Date

Nov 17, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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