VIEW O2 (UDI 180-5057)
Manufactured by Beijing Choice Electronic Technology Co., Ltd.
Device Regulatory Overview
The VIEW O2 (Model/Catalog Number: 180-5057) is a medical device manufactured by Beijing Choice Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 180-5057
- Product Code / EMDN
- DQA
- Device Name
- VIEW O2 FINGER PULSE OXIMETER 180-5057
- Database Sync Date
- 2026-08-09 09:11:07
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 VIEW O2?
The registered manufacturer of record for VIEW O2 is Beijing Choice Electronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for VIEW O2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 180-5057.
What classification code is assigned to this device?
This device is registered under product classification code DQA.
Similar Classification Devices (DQA)
Other Devices by Beijing Choice Electronic Technology Co., Ltd.
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