gudid
Primary ID: 287353401
Depuy Synthes (UDI 287353401)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Depuy Synthes - Primary ID 287353401
Device Regulatory Overview
The Depuy Synthes (Model/Catalog Number: 287353401) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification HTX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 287353401
- Product Code / EMDN
- HTX
- Device Name
- LAT 4MM STRAIGHT PITUITARY
- Database Sync Date
- 2026-08-09 09:02:35
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 Depuy Synthes?
The registered manufacturer of record for Depuy Synthes is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Depuy Synthes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 287353401.
What classification code is assigned to this device?
This device is registered under product classification code HTX.
Similar Classification Devices (HTX)
Other Devices by Avalign Technologies, Inc.
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