gudid
Primary ID: PRT-TDG-25
Protean (UDI PRT-TDG-25)
Manufactured by SKELETAL DYNAMICS L.L.C.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Protean - Primary ID PRT-TDG-25
Device Regulatory Overview
The Protean (Model/Catalog Number: PRT-TDG-25) is a medical device manufactured by SKELETAL DYNAMICS L.L.C.. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PRT-TDG-25
- Product Code / EMDN
- LXH
- Device Name
- PROTEAN, Thread In Drill Guide, 2.5mm
- Database Sync Date
- 2026-08-09 09:39:24
Full Regulatory Attributes
🔒 Token Gated
{
"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 Protean?
The registered manufacturer of record for Protean is SKELETAL DYNAMICS L.L.C..
What is the Primary UDI-DI identifier for Protean?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PRT-TDG-25.
What classification code is assigned to this device?
This device is registered under product classification code LXH.
Similar Classification Devices (LXH)
Other Devices by SKELETAL DYNAMICS L.L.C.
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