GUDIDData
gudid Primary ID: 0221B

Inline Water Trap (UDI 0221B)

Manufactured by WESTMED, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inline Water Trap - Primary ID 0221B

Device Regulatory Overview

The Inline Water Trap (Model/Catalog Number: 0221B) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0221B
Product Code / EMDN
CAW
Device Name
Inline Water Trap, For Oxygen Delivery(This is a component of the Composite Kit for Nationwide Home Med - Part #0837)
Database Sync Date
2026-08-09 09:04:13

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Inline Water Trap?

The registered manufacturer of record for Inline Water Trap is WESTMED, INC..

What is the Primary UDI-DI identifier for Inline Water Trap?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0221B.

What classification code is assigned to this device?

This device is registered under product classification code CAW.

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