TST Spinal System (UDI 08698673462342)
Manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
Device Regulatory Overview
The TST Spinal System (Model/Catalog Number: 20429018035) 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 P09070301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20429018035
- Product Code / EMDN
- P09070301
- Device Name
- CERVICAL SCREW TI 3.5X18
- Database Sync Date
- 2026-08-09 16:29:00
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 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 08698673462342.
What classification code is assigned to this device?
This device is registered under product classification code P09070301.
Similar Classification Devices (P09070301)
Other Devices by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
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