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JERRY Pulse oximeter - Indonesia BPOM Medical Device Registration

JERRY Pulse oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420044. The device is manufactured by SHANXI JERRY MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN SHADY.

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
JERRY Pulse oximeter
Analysis ID: AKL 20502420044

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MAIN SHADY

AR Address

Jalan Biak No. 33 C

Registration Date

Jan 22, 2024

Expiry Date

Jun 09, 2028

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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