gudid
Primary ID: 48970131
Stryker (UDI 48970131)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stryker - Primary ID 48970131
Device Regulatory Overview
The Stryker (Model/Catalog Number: 48970131) 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
- 48970131
- Product Code / EMDN
- HTX
- Device Name
- Pituitary Up-biting 4mm, Non-Bayonetted
- 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 Stryker?
The registered manufacturer of record for Stryker is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Stryker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48970131.
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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