eudamed_udi
Primary ID: 07798034469674
AF Cement VTP (UDI 07798034469674)
Manufactured by Laboratorios SL S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AF Cement VTP - Primary ID 07798034469674
Device Regulatory Overview
The AF Cement VTP (Model/Catalog Number: 880807) 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
- 880807
- Product Code / EMDN
- P099001
- Device Name
- CEMENTO PARA VERTEBROPLASTĂŤA
- Database Sync Date
- 2026-08-09 17:48:16
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 AF Cement VTP?
The registered manufacturer of record for AF Cement VTP is Laboratorios SL S.A..
What is the Primary UDI-DI identifier for AF Cement VTP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07798034469674.
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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