eudamed_udi
Primary ID: 08059591522721
Kit dialisi peritoneale (UDI 08059591522721)
Manufactured by D.R.M. S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kit dialisi peritoneale - Primary ID 08059591522721
Device Regulatory Overview
The Kit dialisi peritoneale (Model/Catalog Number: LC394N) is a medical device manufactured by D.R.M. S.R.L.. This product is indexed under FDA Product Code / Category Classification T0203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LC394N
- Product Code / EMDN
- T0203
- Device Name
- Kit medicazione dialisi sterili
- Database Sync Date
- 2026-08-09 16:29:05
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 Kit dialisi peritoneale?
The registered manufacturer of record for Kit dialisi peritoneale is D.R.M. S.R.L..
What is the Primary UDI-DI identifier for Kit dialisi peritoneale?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059591522721.
What classification code is assigned to this device?
This device is registered under product classification code T0203.
Similar Classification Devices (T0203)
Other Devices by D.R.M. S.R.L.
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