eudamed_udi
Primary ID: 05206756000614
MEDIFORM Medisafe Xlarge (UDI 05206756000614)
Manufactured by MEDIFORM S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDIFORM Medisafe Xlarge - Primary ID 05206756000614
Device Regulatory Overview
The MEDIFORM Medisafe Xlarge (Model/Catalog Number: DME4X10) is a medical device manufactured by MEDIFORM S.A.. This product is indexed under FDA Product Code / Category Classification T04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DME4X10
- Product Code / EMDN
- T04010101
- Device Name
- INCONTINENCE PADS
- Database Sync Date
- 2026-08-09 18:49:07
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 MEDIFORM Medisafe Xlarge?
The registered manufacturer of record for MEDIFORM Medisafe Xlarge is MEDIFORM S.A..
What is the Primary UDI-DI identifier for MEDIFORM Medisafe Xlarge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05206756000614.
What classification code is assigned to this device?
This device is registered under product classification code T04010101.
Similar Classification Devices (T04010101)
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