gudid
Primary ID: 9393
Disposable Anesthesia Circuit (UDI 9393)
Manufactured by WESTMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Disposable Anesthesia Circuit - Primary ID 9393
Device Regulatory Overview
The Disposable Anesthesia Circuit (Model/Catalog Number: 9393) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification OFP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9393
- Product Code / EMDN
- OFP
- Device Name
- Anesthesia, Adult, 72"
- 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 Disposable Anesthesia Circuit?
The registered manufacturer of record for Disposable Anesthesia Circuit is WESTMED, INC..
What is the Primary UDI-DI identifier for Disposable Anesthesia Circuit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9393.
What classification code is assigned to this device?
This device is registered under product classification code OFP.
Similar Classification Devices (OFP)
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