eudamed_udi
Primary ID: 08435225819366
ALAMBRE DE CERCLAJE (UDI 08435225819366)
Manufactured by SURGIVAL CO., S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALAMBRE DE CERCLAJE - Primary ID 08435225819366
Device Regulatory Overview
The ALAMBRE DE CERCLAJE (Model/Catalog Number: C6113001) is a medical device manufactured by SURGIVAL CO., S.A.U.. This product is indexed under FDA Product Code / Category Classification P09120302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C6113001
- Product Code / EMDN
- P09120302
- Device Name
- ALAMBRE DE CERCLAJE
- Database Sync Date
- 2026-08-09 16:49:35
Full Regulatory Attributes
đŸ”’ Token Gated
{
"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 ALAMBRE DE CERCLAJE?
The registered manufacturer of record for ALAMBRE DE CERCLAJE is SURGIVAL CO., S.A.U..
What is the Primary UDI-DI identifier for ALAMBRE DE CERCLAJE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435225819366.
What classification code is assigned to this device?
This device is registered under product classification code P09120302.
Similar Classification Devices (P09120302)
Other Devices by SURGIVAL CO., S.A.U.
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