External aluminium nasal splint (UDI 2060400)
Manufactured by Spiggle & Theis Medizintechnik GmbH
Device Regulatory Overview
The External aluminium nasal splint (Model/Catalog Number: 2060400) 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
- 2060400
- Product Code / EMDN
- EPP
- Device Name
- 66x42x45 mm, large, 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 aluminium nasal splint?
The registered manufacturer of record for External aluminium nasal splint is Spiggle & Theis Medizintechnik GmbH.
What is the Primary UDI-DI identifier for External aluminium nasal splint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2060400.
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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