gudid
Primary ID: 0505586000
PCD SpinePlex (UDI 0505586000)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PCD SpinePlex - Primary ID 0505586000
Device Regulatory Overview
The PCD SpinePlex (Model/Catalog Number: 0505586000) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification LOD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0505586000
- Product Code / EMDN
- LOD
- Device Name
- Precision System without Needle/ Radiopaque Bone Cement
- Database Sync Date
- 2026-08-09 09:53:11
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 PCD SpinePlex?
The registered manufacturer of record for PCD SpinePlex is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for PCD SpinePlex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0505586000.
What classification code is assigned to this device?
This device is registered under product classification code LOD.
Similar Classification Devices (LOD)
Other Devices by STRYKER CORPORATION
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