gudid
Primary ID: 002000
Portex (UDI 002000)
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 002000
Device Regulatory Overview
The Portex (Model/Catalog Number: 002000) is a medical device manufactured by ICU MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002000
- Product Code / EMDN
- BWF
- Device Name
- Database Sync Date
- 2026-08-09 09:34:05
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 002000.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by ICU MEDICAL, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint