eudamed_udi
Primary ID: 08428012302479
Klinidur® cohesive bandage (UDI 08428012302479)
Manufactured by FARMABAN s.a.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Klinidur® cohesive bandage - Primary ID 08428012302479
Device Regulatory Overview
The Klinidur® cohesive bandage (Model/Catalog Number: 40511802) is a medical device manufactured by FARMABAN s.a.. This product is indexed under FDA Product Code / Category Classification M0304010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 40511802
- Product Code / EMDN
- M0304010201
- Device Name
- Venda elástica cohesiva de compresión
- Database Sync Date
- 2026-08-09 16:45:00
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 Klinidur® cohesive bandage?
The registered manufacturer of record for Klinidur® cohesive bandage is FARMABAN s.a..
What is the Primary UDI-DI identifier for Klinidur® cohesive bandage?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08428012302479.
What classification code is assigned to this device?
This device is registered under product classification code M0304010201.
Similar Classification Devices (M0304010201)
Other Devices by FARMABAN s.a.
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