gudid
Primary ID: 05504SP
NA (UDI 05504SP)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 05504SP
Device Regulatory Overview
The NA (Model/Catalog Number: 05504SP) is a medical device manufactured by MEDTRONIC, INC.. This product is indexed under FDA Product Code / Category Classification DRF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 05504SP
- Product Code / EMDN
- DRF
- Device Name
- CABLE 05504SP STERILE UDI
- Database Sync Date
- 2026-08-09 09:17:19
Full Regulatory Attributes
🔒 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 NA?
The registered manufacturer of record for NA is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05504SP.
What classification code is assigned to this device?
This device is registered under product classification code DRF.
Similar Classification Devices (DRF)
Other Devices by MEDTRONIC, INC.
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