gudid
Primary ID: 1002217
Hepa Filter (UDI 1002217)
Manufactured by WESTMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hepa Filter - Primary ID 1002217
Device Regulatory Overview
The Hepa Filter (Model/Catalog Number: 1002217) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1002217
- Product Code / EMDN
- CAH
- Device Name
- Hepa Filter W/CO2 port (TwinMed)
- 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 Hepa Filter?
The registered manufacturer of record for Hepa Filter is WESTMED, INC..
What is the Primary UDI-DI identifier for Hepa Filter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1002217.
What classification code is assigned to this device?
This device is registered under product classification code CAH.
Similar Classification Devices (CAH)
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