eudamed_udi
Primary ID: 05060417201280
Thudicum Speculum No.6 (UDI 05060417201280)
Manufactured by Sheffmed Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Thudicum Speculum No.6 - Primary ID 05060417201280
Device Regulatory Overview
The Thudicum Speculum No.6 (Model/Catalog Number: E10-256) is a medical device manufactured by Sheffmed Limited. This product is indexed under FDA Product Code / Category Classification L149004 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E10-256
- Product Code / EMDN
- L149004
- Device Name
- Retractors - Reusable
- Database Sync Date
- 2026-08-09 17:04:55
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 Thudicum Speculum No.6?
The registered manufacturer of record for Thudicum Speculum No.6 is Sheffmed Limited.
What is the Primary UDI-DI identifier for Thudicum Speculum No.6?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060417201280.
What classification code is assigned to this device?
This device is registered under product classification code L149004.
Similar Classification Devices (L149004)
Other Devices by Sheffmed Limited
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