gudid
Primary ID: 72-3032 BT
Septal splints (UDI 72-3032 BT)
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 72-3032 BT
Device Regulatory Overview
The Septal splints (Model/Catalog Number: 72-3032 BT) is a medical device manufactured by Spiggle & Theis Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification EPP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 72-3032 BT
- Product Code / EMDN
- EPP
- Device Name
- FEP, standard 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 72-3032 BT.
What classification code is assigned to this device?
This device is registered under product classification code EPP.
Similar Classification Devices (EPP)
Other Devices by Spiggle & Theis Medizintechnik GmbH
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