eudamed_udi
Primary ID: 04260148890116
coflex® (UDI 04260148890116)
Manufactured by Paradigm Spine GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for coflex® - Primary ID 04260148890116
Device Regulatory Overview
The coflex® (Model/Catalog Number: UAT10100) is a medical device manufactured by Paradigm Spine GmbH. This product is indexed under FDA Product Code / Category Classification L091103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UAT10100
- Product Code / EMDN
- L091103
- Device Name
- coflex® Bending pliers
- Database Sync Date
- 2026-08-09 17:26:21
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 coflex®?
The registered manufacturer of record for coflex® is Paradigm Spine GmbH.
What is the Primary UDI-DI identifier for coflex®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260148890116.
What classification code is assigned to this device?
This device is registered under product classification code L091103.
Similar Classification Devices (L091103)
Other Devices by Paradigm Spine GmbH
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