TrueLife Oximeter X3 (UDI 06951740540469)
Manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd
Device Regulatory Overview
The TrueLife Oximeter X3 (Model/Catalog Number: JPD-502G) is a medical device manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Z1203020408 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- JPD-502G
- Product Code / EMDN
- Z1203020408
- Device Name
- Pulse Oximeter
- Database Sync Date
- 2026-08-09 17:38:21
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of TrueLife Oximeter X3?
The registered manufacturer of record for TrueLife Oximeter X3 is Shenzhen Jumper Medical Equipment Co.,Ltd.
What is the Primary UDI-DI identifier for TrueLife Oximeter X3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951740540469.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020408.
Similar Classification Devices (Z1203020408)
Other Devices by Shenzhen Jumper Medical Equipment Co.,Ltd
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