eudamed_udi
Primary ID: 80518846853736
Compresse di Garza Tagliata (UDI 80518846853736)
Manufactured by RAYS S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Compresse di Garza Tagliata - Primary ID 80518846853736
Device Regulatory Overview
The Compresse di Garza Tagliata (Model/Catalog Number: K23X3N1NZB) is a medical device manufactured by RAYS S.p.A.. This product is indexed under FDA Product Code / Category Classification M0201010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K23X3N1NZB
- Product Code / EMDN
- M0201010102
- Device Name
- Non Sterile Cut Gauze
- Database Sync Date
- 2026-08-09 16:45:40
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 Compresse di Garza Tagliata?
The registered manufacturer of record for Compresse di Garza Tagliata is RAYS S.p.A..
What is the Primary UDI-DI identifier for Compresse di Garza Tagliata?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80518846853736.
What classification code is assigned to this device?
This device is registered under product classification code M0201010102.
Similar Classification Devices (M0201010102)
Other Devices by RAYS S.p.A.
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