eudamed_udi
Primary ID: 04042809796087
Leukoplast® (UDI 04042809796087)
Manufactured by BSN medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Leukoplast® - Primary ID 04042809796087
Device Regulatory Overview
The Leukoplast® (Model/Catalog Number: 71234-00) is a medical device manufactured by BSN medical GmbH. This product is indexed under FDA Product Code / Category Classification M0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 71234-00
- Product Code / EMDN
- M0201020102
- Device Name
- Leukoplast® compress cotton gauze
- Database Sync Date
- 2026-08-09 16:30:03
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 Leukoplast®?
The registered manufacturer of record for Leukoplast® is BSN medical GmbH.
What is the Primary UDI-DI identifier for Leukoplast®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04042809796087.
What classification code is assigned to this device?
This device is registered under product classification code M0201020102.
Similar Classification Devices (M0201020102)
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