eudamed_udi
Primary ID: 05904754914734
DynamX System (UDI 05904754914734)
Manufactured by Syntropiq s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DynamX System - Primary ID 05904754914734
Device Regulatory Overview
The DynamX System (Model/Catalog Number: 4221560013) is a medical device manufactured by Syntropiq s.r.o.. This product is indexed under FDA Product Code / Category Classification P09070101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4221560013
- Product Code / EMDN
- P09070101
- Device Name
- Ultra Lateral Fusion Cage, Size: 21x56x13 mm, Angulation: 00° , Anatomic, Trabecular
- Database Sync Date
- 2026-08-09 16:28:50
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 DynamX System?
The registered manufacturer of record for DynamX System is Syntropiq s.r.o..
What is the Primary UDI-DI identifier for DynamX System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904754914734.
What classification code is assigned to this device?
This device is registered under product classification code P09070101.
Similar Classification Devices (P09070101)
Other Devices by Syntropiq s.r.o.
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