eudamed_udi
Primary ID: 05033955056063
Swann-Morton (UDI 05033955056063)
Manufactured by Swann-Morton Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Swann-Morton - Primary ID 05033955056063
Device Regulatory Overview
The Swann-Morton (Model/Catalog Number: 5606 - No. 20 Non Sterile Kleen Blade Management System) is a medical device manufactured by Swann-Morton Ltd. This product is indexed under FDA Product Code / Category Classification V010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5606 - No. 20 Non Sterile Kleen Blade Management System
- Product Code / EMDN
- V010302
- Device Name
- Swann-Morton Non Sterile Kleen Blade Management System
- Database Sync Date
- 2026-08-09 16:46:27
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 Swann-Morton?
The registered manufacturer of record for Swann-Morton is Swann-Morton Ltd.
What is the Primary UDI-DI identifier for Swann-Morton?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05033955056063.
What classification code is assigned to this device?
This device is registered under product classification code V010302.
Similar Classification Devices (V010302)
Other Devices by Swann-Morton Ltd
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