eudamed_udi
Primary ID: 04250816975900
Stem Drill L110 (UDI 04250816975900)
Manufactured by OHST Medizintechnik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stem Drill L110 - Primary ID 04250816975900
Device Regulatory Overview
The Stem Drill L110 (Model/Catalog Number: 521-116) is a medical device manufactured by OHST Medizintechnik AG. This product is indexed under FDA Product Code / Category Classification L091102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 521-116
- Product Code / EMDN
- L091102
- Device Name
- IIa_Drill
- Database Sync Date
- 2026-08-09 16:29:18
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 Stem Drill L110?
The registered manufacturer of record for Stem Drill L110 is OHST Medizintechnik AG.
What is the Primary UDI-DI identifier for Stem Drill L110?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250816975900.
What classification code is assigned to this device?
This device is registered under product classification code L091102.
Similar Classification Devices (L091102)
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