Pulse Oximeter (UDI 06947832502453)
Manufactured by Shenzhen Aeon Technology Co., Ltd.
Device Regulatory Overview
The Pulse Oximeter (Model/Catalog Number: A300) is a medical device manufactured by Shenzhen Aeon Technology 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
- A300
- Product Code / EMDN
- Z1203020408
- Device Name
- Pulse Oximeter
- Database Sync Date
- 2026-08-09 16:45:44
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 Pulse Oximeter?
The registered manufacturer of record for Pulse Oximeter is Shenzhen Aeon Technology Co., Ltd..
What is the Primary UDI-DI identifier for Pulse Oximeter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06947832502453.
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 Aeon Technology Co., Ltd.
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