eudamed_udi
Primary ID: 06939488524422
Solid Vertebral Drill (UDI 06939488524422)
Manufactured by Dragon Crown Medical Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solid Vertebral Drill - Primary ID 06939488524422
Device Regulatory Overview
The Solid Vertebral Drill (Model/Catalog Number: LG08268) is a medical device manufactured by Dragon Crown Medical Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification P099002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LG08268
- Product Code / EMDN
- P099002
- Device Name
- Vertebral Forming Unitized Surgical Instruments and Vertebroplasty Toolkit
- Database Sync Date
- 2026-08-09 16:29:47
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 Solid Vertebral Drill?
The registered manufacturer of record for Solid Vertebral Drill is Dragon Crown Medical Co.,Ltd..
What is the Primary UDI-DI identifier for Solid Vertebral Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06939488524422.
What classification code is assigned to this device?
This device is registered under product classification code P099002.
Similar Classification Devices (P099002)
Other Devices by Dragon Crown Medical Co.,Ltd.
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