gudid
Primary ID: 4806L50
NA (UDI 4806L50)
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 4806L50
Device Regulatory Overview
The NA (Model/Catalog Number: 4806L50) is a medical device manufactured by MEDTRONIC, INC.. This product is indexed under FDA Product Code / Category Classification LPB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4806L50
- Product Code / EMDN
- LPB
- Device Name
- RMT CNTRL 4806L50 FT SWTCH 50 FT
- Database Sync Date
- 2026-08-09 09:17:19
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 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 4806L50.
What classification code is assigned to this device?
This device is registered under product classification code LPB.
Similar Classification Devices (LPB)
Other Devices by MEDTRONIC, INC.
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