gudid
Primary ID: 210-P20004
KeriFlex (UDI 210-P20004)
Manufactured by Keri Medical SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KeriFlex - Primary ID 210-P20004
Device Regulatory Overview
The KeriFlex (Model/Catalog Number: 210-P20004) is a medical device manufactured by Keri Medical SA. This product is indexed under FDA Product Code / Category Classification KYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 210-P20004
- Product Code / EMDN
- KYJ
- 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 KeriFlex?
The registered manufacturer of record for KeriFlex is Keri Medical SA.
What is the Primary UDI-DI identifier for KeriFlex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 210-P20004.
What classification code is assigned to this device?
This device is registered under product classification code KYJ.
Similar Classification Devices (KYJ)
Other Devices by Keri Medical SA
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JSON API Endpoint