TST Cannulated Screws System (UDI 08680858455317)
Manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
Device Regulatory Overview
The TST Cannulated Screws System (Model/Catalog Number: 23821055035) 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 P09120603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 23821055035
- Product Code / EMDN
- P09120603
- Device Name
- CANNULATED BEAMING SCREW (FULL THRD) 4X55 MM
- Database Sync Date
- 2026-08-09 16:29:02
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 Cannulated Screws System?
The registered manufacturer of record for TST Cannulated Screws System is TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ..
What is the Primary UDI-DI identifier for TST Cannulated Screws System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680858455317.
What classification code is assigned to this device?
This device is registered under product classification code P09120603.
Similar Classification Devices (P09120603)
Other Devices by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
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