eudamed_udi
Primary ID: 00817906028553
CoLink Afx (UDI 00817906028553)
Manufactured by In2Bones, USA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CoLink Afx - Primary ID 00817906028553
Device Regulatory Overview
The CoLink Afx (Model/Catalog Number: P07 N1301) is a medical device manufactured by In2Bones, USA. This product is indexed under FDA Product Code / Category Classification L091104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P07 N1301
- Product Code / EMDN
- L091104
- Device Name
- Ankle Fracture Non-Sterile Instruments (Trials), Active
- 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 CoLink Afx?
The registered manufacturer of record for CoLink Afx is In2Bones, USA.
What is the Primary UDI-DI identifier for CoLink Afx?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00817906028553.
What classification code is assigned to this device?
This device is registered under product classification code L091104.
Similar Classification Devices (L091104)
Other Devices by In2Bones, USA
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