eudamed_udi
Primary ID: 05060417201822
Lucs Forceps Sterile (UDI 05060417201822)
Manufactured by Sheffmed Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lucs Forceps Sterile - Primary ID 05060417201822
Device Regulatory Overview
The Lucs Forceps Sterile (Model/Catalog Number: TE12-158S) is a medical device manufactured by Sheffmed Limited. This product is indexed under FDA Product Code / Category Classification Q0399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TE12-158S
- Product Code / EMDN
- Q0399
- Device Name
- Forceps - Sterile
- Database Sync Date
- 2026-08-09 16:51:27
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 Lucs Forceps Sterile?
The registered manufacturer of record for Lucs Forceps Sterile is Sheffmed Limited.
What is the Primary UDI-DI identifier for Lucs Forceps Sterile?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060417201822.
What classification code is assigned to this device?
This device is registered under product classification code Q0399.
Similar Classification Devices (Q0399)
Other Devices by Sheffmed Limited
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