GUDIDData
eudamed_udi Primary ID: 08699931012644

TST External Fixator System (UDI 08699931012644)

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 External Fixator System - Primary ID 08699931012644

Device Regulatory Overview

The TST External Fixator System (Model/Catalog Number: 52650000005) 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 P09120499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
52650000005
Product Code / EMDN
P09120499
Device Name
FEMALE SUPPORT 5 HOLES
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of TST External Fixator System?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699931012644.

What classification code is assigned to this device?

This device is registered under product classification code P09120499.

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