gudid
Primary ID: UFR102
ZKZO (UDI UFR102)
Manufactured by Shenzhen Urion Technology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZKZO - Primary ID UFR102
Device Regulatory Overview
The ZKZO (Model/Catalog Number: UFR102) is a medical device manufactured by Shenzhen Urion Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification FLL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UFR102
- Product Code / EMDN
- FLL
- Device Name
- Database Sync Date
- 2026-08-09 09:05:25
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 ZKZO?
The registered manufacturer of record for ZKZO is Shenzhen Urion Technology Co., Ltd.
What is the Primary UDI-DI identifier for ZKZO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UFR102.
What classification code is assigned to this device?
This device is registered under product classification code FLL.
Similar Classification Devices (FLL)
Other Devices by Shenzhen Urion Technology Co., Ltd
Programmatic Export
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