eudamed_udi
Primary ID: 05206756001048
MEDIFORM Medipant Maxi Medium (UDI 05206756001048)
Manufactured by MEDIFORM S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDIFORM Medipant Maxi Medium - Primary ID 05206756001048
Device Regulatory Overview
The MEDIFORM Medipant Maxi Medium (Model/Catalog Number: PME228) is a medical device manufactured by MEDIFORM S.A.. This product is indexed under FDA Product Code / Category Classification T99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PME228
- Product Code / EMDN
- T99
- Device Name
- incontinence pants
- Database Sync Date
- 2026-08-09 18:27:33
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 Medipant Maxi Medium?
The registered manufacturer of record for MEDIFORM Medipant Maxi Medium is MEDIFORM S.A..
What is the Primary UDI-DI identifier for MEDIFORM Medipant Maxi Medium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05206756001048.
What classification code is assigned to this device?
This device is registered under product classification code T99.
Similar Classification Devices (T99)
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