gudid
Primary ID: 2042025
Septal splints (UDI 2042025)
Manufactured by Spiggle & Theis Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Septal splints - Primary ID 2042025
Device Regulatory Overview
The Septal splints (Model/Catalog Number: 2042025) is a medical device manufactured by Spiggle & Theis Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification LYA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2042025
- Product Code / EMDN
- LYA
- Device Name
- FEP, large 0.25 mm, sterile, 5 pairs/box
- Database Sync Date
- 2026-08-09 09:11:39
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 Septal splints?
The registered manufacturer of record for Septal splints is Spiggle & Theis Medizintechnik GmbH.
What is the Primary UDI-DI identifier for Septal splints?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2042025.
What classification code is assigned to this device?
This device is registered under product classification code LYA.
Similar Classification Devices (LYA)
Other Devices by Spiggle & Theis Medizintechnik GmbH
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