eudamed_udi
Primary ID: 05063250549472
Tesco Crepe Bandage (UDI 05063250549472)
Manufactured by TOILETRY SALES LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tesco Crepe Bandage - Primary ID 05063250549472
Device Regulatory Overview
The Tesco Crepe Bandage (Model/Catalog Number: 5381) is a medical device manufactured by TOILETRY SALES LIMITED. This product is indexed under FDA Product Code / Category Classification M030402020103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5381
- Product Code / EMDN
- M030402020103
- Device Name
- Stretch Bandage
- Database Sync Date
- 2026-08-09 17:24:57
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 Tesco Crepe Bandage?
The registered manufacturer of record for Tesco Crepe Bandage is TOILETRY SALES LIMITED.
What is the Primary UDI-DI identifier for Tesco Crepe Bandage?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05063250549472.
What classification code is assigned to this device?
This device is registered under product classification code M030402020103.
Similar Classification Devices (M030402020103)
Other Devices by TOILETRY SALES LIMITED
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