Ortholox® Sternum Closure Instruments - Container(Empty) (UDI 08682320050198)
Manufactured by ORTOLOG MEDİKAL SANAYİ VE TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The Ortholox® Sternum Closure Instruments - Container(Empty) (Model/Catalog Number: 12-900-000) is a medical device manufactured by ORTOLOG MEDİKAL SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification L070799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12-900-000
- Product Code / EMDN
- L070799
- Device Name
- Non-Sterile Reusable Surgical Instruments - Sets
- Database Sync Date
- 2026-08-09 18:12:47
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 Ortholox® Sternum Closure Instruments - Container(Empty)?
The registered manufacturer of record for Ortholox® Sternum Closure Instruments - Container(Empty) is ORTOLOG MEDİKAL SANAYİ VE TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Ortholox® Sternum Closure Instruments - Container(Empty)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682320050198.
What classification code is assigned to this device?
This device is registered under product classification code L070799.
Similar Classification Devices (L070799)
Other Devices by ORTOLOG MEDİKAL SANAYİ VE TİCARET ANONİM ŞİRKETİ
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