eudamed_udi
Primary ID: 42514018019702
Osteotome M (UDI 42514018019702)
Manufactured by endocon GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Osteotome M - Primary ID 42514018019702
Device Regulatory Overview
The Osteotome M (Model/Catalog Number: 00200731 endocon catalogue) is a medical device manufactured by endocon GmbH. This product is indexed under FDA Product Code / Category Classification L090401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00200731 endocon catalogue
- Product Code / EMDN
- L090401
- Device Name
- Revisionsinstrumentensystem
- Database Sync Date
- 2026-08-09 16:28:47
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 Osteotome M?
The registered manufacturer of record for Osteotome M is endocon GmbH.
What is the Primary UDI-DI identifier for Osteotome M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42514018019702.
What classification code is assigned to this device?
This device is registered under product classification code L090401.
Similar Classification Devices (L090401)
Other Devices by endocon GmbH
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