gudid
Primary ID: NA
Depth Gauge O-Ring, Modified (UDI NA)
Manufactured by TOBY ORTHOPAEDICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Depth Gauge O-Ring, Modified - Primary ID NA
Device Regulatory Overview
The Depth Gauge O-Ring, Modified (Model/Catalog Number: NA) is a medical device manufactured by TOBY ORTHOPAEDICS. This product is indexed under FDA Product Code / Category Classification HTJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NA
- Product Code / EMDN
- HTJ
- Device Name
- Component of Depth Gauge.
- 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 Depth Gauge O-Ring, Modified?
The registered manufacturer of record for Depth Gauge O-Ring, Modified is TOBY ORTHOPAEDICS.
What is the Primary UDI-DI identifier for Depth Gauge O-Ring, Modified?
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 HTJ.
Similar Classification Devices (HTJ)
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