eudamed_udi
Primary ID: 00810832030454
OrthAlign Plus (UDI 00810832030454)
Manufactured by OrthAlign, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OrthAlign Plus - Primary ID 00810832030454
Device Regulatory Overview
The OrthAlign Plus (Model/Catalog Number: 403468) is a medical device manufactured by OrthAlign, Inc. This product is indexed under FDA Product Code / Category Classification L0908 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 403468
- Product Code / EMDN
- L0908
- Device Name
- 4mm Dia Drill Guide, HipAlign
- Database Sync Date
- 2026-08-09 16:46:06
Full Regulatory Attributes
đź”’ 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 OrthAlign Plus?
The registered manufacturer of record for OrthAlign Plus is OrthAlign, Inc.
What is the Primary UDI-DI identifier for OrthAlign Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810832030454.
What classification code is assigned to this device?
This device is registered under product classification code L0908.
Similar Classification Devices (L0908)
Other Devices by OrthAlign, Inc
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