gudid
Primary ID: 262PR102004
Lid KeriFlex (UDI 262PR102004)
Manufactured by Keri Medical SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lid KeriFlex - Primary ID 262PR102004
Device Regulatory Overview
The Lid KeriFlex (Model/Catalog Number: 262PR102004) is a medical device manufactured by Keri Medical SA. This product is indexed under FDA Product Code / Category Classification LRP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 262PR102004
- Product Code / EMDN
- LRP
- Device Name
- Database Sync Date
- 2026-08-09 09:16:08
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 Lid KeriFlex?
The registered manufacturer of record for Lid KeriFlex is Keri Medical SA.
What is the Primary UDI-DI identifier for Lid KeriFlex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 262PR102004.
What classification code is assigned to this device?
This device is registered under product classification code LRP.
Similar Classification Devices (LRP)
Other Devices by Keri Medical SA
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