gudid
Primary ID: 307F1
Freezor (UDI 307F1)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freezor - Primary ID 307F1
Device Regulatory Overview
The Freezor (Model/Catalog Number: 307F1) 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
- 307F1
- Product Code / EMDN
- LPB
- Device Name
- CATHETER 307F1 FREEZOR1 SHT RED 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?
The registered manufacturer of record for Freezor is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for Freezor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 307F1.
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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