gudid
Primary ID: 100/856/100
Portex (UDI 100/856/100)
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 100/856/100
Device Regulatory Overview
The Portex (Model/Catalog Number: 100/856/100) is a medical device manufactured by ICU MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification BTO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100/856/100
- Product Code / EMDN
- BTO
- Device Name
- Database Sync Date
- 2026-08-09 09:16:52
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 100/856/100.
What classification code is assigned to this device?
This device is registered under product classification code BTO.
Similar Classification Devices (BTO)
Other Devices by ICU MEDICAL, INC.
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