eudamed_udi
Primary ID: 10886705003068
RIGIDFIX Femoral Rod (UDI 10886705003068)
Manufactured by Medos International SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIGIDFIX Femoral Rod - Primary ID 10886705003068
Device Regulatory Overview
The RIGIDFIX Femoral Rod (Model/Catalog Number: 213712) is a medical device manufactured by Medos International SARL. This product is indexed under FDA Product Code / Category Classification Z12139099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 213712
- Product Code / EMDN
- Z12139099
- Device Name
- Rigidfix, Femoral, Rod, Restore, Aimer, Tibial, Guide
- Database Sync Date
- 2026-08-09 16:29:15
Full Regulatory Attributes
đź”’ 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 RIGIDFIX Femoral Rod?
The registered manufacturer of record for RIGIDFIX Femoral Rod is Medos International SARL.
What is the Primary UDI-DI identifier for RIGIDFIX Femoral Rod?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10886705003068.
What classification code is assigned to this device?
This device is registered under product classification code Z12139099.
Similar Classification Devices (Z12139099)
Other Devices by Medos International SARL
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