gudid
Primary ID: 229F5
Freezor MAX (UDI 229F5)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freezor MAX - Primary ID 229F5
Device Regulatory Overview
The Freezor MAX (Model/Catalog Number: 229F5) 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
- 229F5
- Product Code / EMDN
- LPB
- Device Name
- CATH 229F5 FREEZOR MAX5 SURGICAL LG 9F
- 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 MAX?
The registered manufacturer of record for Freezor MAX is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for Freezor MAX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 229F5.
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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