eudamed_udi
Primary ID: 05206756001574
MEDIFORM Medislip Maxi Large (UDI 05206756001574)
Manufactured by MEDIFORM S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDIFORM Medislip Maxi Large - Primary ID 05206756001574
Device Regulatory Overview
The MEDIFORM Medislip Maxi Large (Model/Catalog Number: DME3X26) 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
- DME3X26
- Product Code / EMDN
- T04010101
- Device Name
- INCONTINENCE PADS
- Database Sync Date
- 2026-08-09 17:35:51
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MEDIFORM Medislip Maxi Large?
The registered manufacturer of record for MEDIFORM Medislip Maxi Large is MEDIFORM S.A..
What is the Primary UDI-DI identifier for MEDIFORM Medislip Maxi Large?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05206756001574.
What classification code is assigned to this device?
This device is registered under product classification code T04010101.
Similar Classification Devices (T04010101)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint