TST Tibia Plates (UDI 08699931013863)
Manufactured by TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ.
Device Regulatory Overview
The TST Tibia Plates (Model/Catalog Number: 30127000114) 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
- 30127000114
- Product Code / EMDN
- P09120503
- Device Name
- LC DCP INTERLOCK.CONICAL TIBIAL PLATE 14 HOLES
- Database Sync Date
- 2026-08-09 16:28:48
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 Tibia Plates?
The registered manufacturer of record for TST Tibia Plates is TST RAKOR VE TIBBİ ALETLER SAN.VE TİC.LTD.ŞTİ..
What is the Primary UDI-DI identifier for TST Tibia Plates?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08699931013863.
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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