Essere Benessere Assorbenti Lady Maxi Night (UDI 08058776693300)
Manufactured by C.I.M. Cardificio Italiano S.p.A.
Device Regulatory Overview
The Essere Benessere Assorbenti Lady Maxi Night (Model/Catalog Number: 225820) 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
- 225820
- Product Code / EMDN
- T0499
- Device Name
- Assorbenti La Nuova Pharmacia Extra
- Database Sync Date
- 2026-08-09 16:44:58
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 Essere Benessere Assorbenti Lady Maxi Night?
The registered manufacturer of record for Essere Benessere Assorbenti Lady Maxi Night is C.I.M. Cardificio Italiano S.p.A..
What is the Primary UDI-DI identifier for Essere Benessere Assorbenti Lady Maxi Night?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058776693300.
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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