eudamed_udi
Primary ID: 42514018002490
Canulated Drill (UDI 42514018002490)
Manufactured by endocon GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Canulated Drill - Primary ID 42514018002490
Device Regulatory Overview
The Canulated Drill (Model/Catalog Number: FR-060 endocon catalogue) is a medical device manufactured by endocon GmbH. This product is indexed under FDA Product Code / Category Classification L091101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FR-060 endocon catalogue
- Product Code / EMDN
- L091101
- Device Name
- OrthoClast
- Database Sync Date
- 2026-08-09 16:29:03
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 Canulated Drill?
The registered manufacturer of record for Canulated Drill is endocon GmbH.
What is the Primary UDI-DI identifier for Canulated Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42514018002490.
What classification code is assigned to this device?
This device is registered under product classification code L091101.
Similar Classification Devices (L091101)
Other Devices by endocon GmbH
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