gudid
Primary ID: A3559-25
Portex (UDI A3559-25)
Manufactured by ICU MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Portex - Primary ID A3559-25
Device Regulatory Overview
The Portex (Model/Catalog Number: A3559-25) is a medical device manufactured by ICU MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification CAZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A3559-25
- Product Code / EMDN
- CAZ
- Device Name
- Database Sync Date
- 2026-08-09 09:20:08
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 Portex?
The registered manufacturer of record for Portex is ICU MEDICAL, INC..
What is the Primary UDI-DI identifier for Portex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A3559-25.
What classification code is assigned to this device?
This device is registered under product classification code CAZ.
Similar Classification Devices (CAZ)
Other Devices by ICU MEDICAL, INC.
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