eudamed_udi
Primary ID: 07798034467984
Genta C-ment® (UDI 07798034467984)
Manufactured by Laboratorios SL S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Genta C-ment® - Primary ID 07798034467984
Device Regulatory Overview
The Genta C-ment® (Model/Catalog Number: 880473) is a medical device manufactured by Laboratorios SL S.A.. This product is indexed under FDA Product Code / Category Classification P099001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 880473
- Product Code / EMDN
- P099001
- Device Name
- CEMENTO ORTOPÉDICO CON ANTIBIÓTICO
- Database Sync Date
- 2026-08-09 17:04:22
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 Genta C-ment®?
The registered manufacturer of record for Genta C-ment® is Laboratorios SL S.A..
What is the Primary UDI-DI identifier for Genta C-ment®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07798034467984.
What classification code is assigned to this device?
This device is registered under product classification code P099001.
Similar Classification Devices (P099001)
Other Devices by Laboratorios SL S.A.
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