GUDIDData
eudamed_udi Primary ID: 08698673470675

TST Spinal System (UDI 08698673470675)

Manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TST Spinal System - Primary ID 08698673470675

Device Regulatory Overview

The TST Spinal System (Model/Catalog Number: 74221450650) is a medical device manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.. This product is indexed under FDA Product Code / Category Classification P09070302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
74221450650
Product Code / EMDN
P09070302
Device Name
INT. LOCK. SPONDYL. SCREW Ø 6.5 MMX45 MM
Database Sync Date
2026-08-09 16:28:58

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of TST Spinal System?

The registered manufacturer of record for TST Spinal System is TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ..

What is the Primary UDI-DI identifier for TST Spinal System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698673470675.

What classification code is assigned to this device?

This device is registered under product classification code P09070302.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint