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JUMPER Fingertip Pulse Oximeter - Indonesia BPOM Medical Device Registration

JUMPER Fingertip Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420380. The device is manufactured by SHENZHEN JUMPER MEDICAL EQUIPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ASA PRATAMA PARTNERS.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
JUMPER Fingertip Pulse Oximeter
Analysis ID: AKL 20502420380

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

Oct 03, 2024

Expiry Date

Dec 23, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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