Ortimplant (UDI 08680941164508)
Manufactured by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi
Device Regulatory Overview
The Ortimplant (Model/Catalog Number: O400 03 011 1019) is a medical device manufactured by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi. This product is indexed under FDA Product Code / Category Classification P09120302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- O400 03 011 1019
- Product Code / EMDN
- P09120302
- Device Name
- SERKLAJ TELİ ÖLÇÜ ÇELİK (CERCLAGE WIRE SIZE SS) 1 MM
- Database Sync Date
- 2026-08-09 16:46:10
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 Ortimplant?
The registered manufacturer of record for Ortimplant is Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi.
What is the Primary UDI-DI identifier for Ortimplant?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680941164508.
What classification code is assigned to this device?
This device is registered under product classification code P09120302.
Similar Classification Devices (P09120302)
Other Devices by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi
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