eudamed_udi
Primary ID: 04052024062812
Fußschiene, zur Korrekturkontrolle (UDI 04052024062812)
Manufactured by INTERCUS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fußschiene, zur Korrekturkontrolle - Primary ID 04052024062812
Device Regulatory Overview
The Fußschiene, zur Korrekturkontrolle (Model/Catalog Number: 750.109903) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification L091099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 750.109903
- Product Code / EMDN
- L091099
- Device Name
- Hilfsmittel zum Längen- und Positionsvergleich
- Database Sync Date
- 2026-08-09 17:49:17
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 Fußschiene, zur Korrekturkontrolle?
The registered manufacturer of record for Fußschiene, zur Korrekturkontrolle is INTERCUS GmbH.
What is the Primary UDI-DI identifier for Fußschiene, zur Korrekturkontrolle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024062812.
What classification code is assigned to this device?
This device is registered under product classification code L091099.
Similar Classification Devices (L091099)
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