eudamed_udi
Primary ID: 00000003485057
WILKO CREPE BANDAGE (UDI 00000003485057)
Manufactured by TOILETRY SALES LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WILKO CREPE BANDAGE - Primary ID 00000003485057
Device Regulatory Overview
The WILKO CREPE BANDAGE (Model/Catalog Number: 1356) 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
- 1356
- Product Code / EMDN
- M030402020103
- Device Name
- Stretch Bandage
- Database Sync Date
- 2026-08-09 16:29:39
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 WILKO CREPE BANDAGE?
The registered manufacturer of record for WILKO CREPE BANDAGE is TOILETRY SALES LIMITED.
What is the Primary UDI-DI identifier for WILKO CREPE BANDAGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00000003485057.
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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