gudid
Primary ID: 67-2450-0105-51
Medfusion (UDI 67-2450-0105-51)
Manufactured by ICU MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medfusion - Primary ID 67-2450-0105-51
Device Regulatory Overview
The Medfusion (Model/Catalog Number: 67-2450-0105-51) is a medical device manufactured by ICU MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification MRZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 67-2450-0105-51
- Product Code / EMDN
- MRZ
- Device Name
- Database Sync Date
- 2026-08-09 09:31:01
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 Medfusion?
The registered manufacturer of record for Medfusion is ICU MEDICAL, INC..
What is the Primary UDI-DI identifier for Medfusion?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 67-2450-0105-51.
What classification code is assigned to this device?
This device is registered under product classification code MRZ.
Similar Classification Devices (MRZ)
Other Devices by ICU MEDICAL, INC.
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