External thermoplastic nasal splint (UDI 2051000)
Manufactured by Spiggle & Theis Medizintechnik GmbH
Device Regulatory Overview
The External thermoplastic nasal splint (Model/Catalog Number: 2051000) 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
- 2051000
- Product Code / EMDN
- EPP
- Device Name
- 80x50 mm, cuttable, 1.6 mm self-adhesive, 10 pieces/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 External thermoplastic nasal splint?
The registered manufacturer of record for External thermoplastic nasal splint is Spiggle & Theis Medizintechnik GmbH.
What is the Primary UDI-DI identifier for External thermoplastic nasal splint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2051000.
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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