gudid
Primary ID: 0909200050
SpineJack (UDI 0909200050)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SpineJack - Primary ID 0909200050
Device Regulatory Overview
The SpineJack (Model/Catalog Number: 0909200050) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification NDN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0909200050
- Product Code / EMDN
- NDN
- Device Name
- EXPANSION KIT 5.0MM
- Database Sync Date
- 2026-08-09 09:33:50
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 SpineJack?
The registered manufacturer of record for SpineJack is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for SpineJack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0909200050.
What classification code is assigned to this device?
This device is registered under product classification code NDN.
Similar Classification Devices (NDN)
Other Devices by STRYKER CORPORATION
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