eudamed_udi
Primary ID: 08800342283749
122 KS Drill (UDI 08800342283749)
Manufactured by OSSTEM IMPLANT Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 122 KS Drill - Primary ID 08800342283749
Device Regulatory Overview
The 122 KS Drill (Model/Catalog Number: O122KSD5510) is a medical device manufactured by OSSTEM IMPLANT Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L159099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- O122KSD5510
- Product Code / EMDN
- L159099
- Device Name
- Surgical Drill System
- 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 122 KS Drill?
The registered manufacturer of record for 122 KS Drill is OSSTEM IMPLANT Co., Ltd..
What is the Primary UDI-DI identifier for 122 KS Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800342283749.
What classification code is assigned to this device?
This device is registered under product classification code L159099.
Similar Classification Devices (L159099)
Other Devices by OSSTEM IMPLANT Co., Ltd.
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