eudamed_udi
Primary ID: 08003100833136
Selex Lady Super (UDI 08003100833136)
Manufactured by C.I.M. Cardificio Italiano S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Selex Lady Super - Primary ID 08003100833136
Device Regulatory Overview
The Selex Lady Super (Model/Catalog Number: 225345) is a medical device manufactured by C.I.M. Cardificio Italiano S.p.A.. This product is indexed under FDA Product Code / Category Classification T0499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 225345
- Product Code / EMDN
- T0499
- Device Name
- Assorbenti La Nuova Pharmacia Extra
- Database Sync Date
- 2026-08-09 16:29:56
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 Selex Lady Super?
The registered manufacturer of record for Selex Lady Super is C.I.M. Cardificio Italiano S.p.A..
What is the Primary UDI-DI identifier for Selex Lady Super?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08003100833136.
What classification code is assigned to this device?
This device is registered under product classification code T0499.
Similar Classification Devices (T0499)
Other Devices by C.I.M. Cardificio Italiano S.p.A.
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