gudid
Primary ID: 10035469
Dual--Lumen Cannula (UDI 10035469)
Manufactured by WESTMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dual--Lumen Cannula - Primary ID 10035469
Device Regulatory Overview
The Dual--Lumen Cannula (Model/Catalog Number: 10035469) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10035469
- Product Code / EMDN
- CAT
- Device Name
- Dual-Lumen Nasal Cannula, 3', Caire
- Database Sync Date
- 2026-08-09 09:04:13
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 Dual--Lumen Cannula?
The registered manufacturer of record for Dual--Lumen Cannula is WESTMED, INC..
What is the Primary UDI-DI identifier for Dual--Lumen Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10035469.
What classification code is assigned to this device?
This device is registered under product classification code CAT.
Similar Classification Devices (CAT)
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