TST Femur Plates (UDI 08699931016215)
Manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
Device Regulatory Overview
The TST Femur Plates (Model/Catalog Number: 31626700007) 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 P09120503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31626700007
- Product Code / EMDN
- P09120503
- Device Name
- PROX. FEMUR LOCK. PLATECONICAL HOLES TI L 7 H
- Database Sync Date
- 2026-08-09 16:28:45
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 Femur Plates?
The registered manufacturer of record for TST Femur Plates is TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ..
What is the Primary UDI-DI identifier for TST Femur Plates?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699931016215.
What classification code is assigned to this device?
This device is registered under product classification code P09120503.
Similar Classification Devices (P09120503)
Other Devices by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
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