gudid
Primary ID: NA
Cross Element Guide Retainer (UDI NA)
Manufactured by TOBY ORTHOPAEDICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cross Element Guide Retainer - Primary ID NA
Device Regulatory Overview
The Cross Element Guide Retainer (Model/Catalog Number: NA) is a medical device manufactured by TOBY ORTHOPAEDICS. This product is indexed under FDA Product Code / Category Classification GCZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NA
- Product Code / EMDN
- GCZ
- Device Name
- Guides are stainless steel parts of various designs that allow various drill diameters. Some guides are laser weld assemblies with a handle, and others are threaded to screw into plates.
- Database Sync Date
- 2026-08-09 09:40:13
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 Cross Element Guide Retainer?
The registered manufacturer of record for Cross Element Guide Retainer is TOBY ORTHOPAEDICS.
What is the Primary UDI-DI identifier for Cross Element Guide Retainer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NA.
What classification code is assigned to this device?
This device is registered under product classification code GCZ.
Similar Classification Devices (GCZ)
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