gudid
Primary ID: 227F5
Freezor Xtra (UDI 227F5)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freezor Xtra - Primary ID 227F5
Device Regulatory Overview
The Freezor Xtra (Model/Catalog Number: 227F5) 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
- 227F5
- Product Code / EMDN
- LPB
- Device Name
- CATH 227F5 FREEZOR XTRA5 SURGICAL LG 7F
- Database Sync Date
- 2026-08-09 09:36:27
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 Freezor Xtra?
The registered manufacturer of record for Freezor Xtra is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for Freezor Xtra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 227F5.
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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