gudid Primary ID: 230-1092-Y3K

Caplugs/Evergreen (UDI 230-1092-Y3K)

Manufactured by CAPlugs

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Caplugs/Evergreen (Model/Catalog Number: 230-1092-Y3K) is a medical device manufactured by CAPlugs. This product is indexed under FDA Product Code / Category Classification JQW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 230-1092-Y3K
Product Code / EMDN: JQW
Device Name: P TIP 250-500UL OX AB PF QP
Database Sync Date: 2026-08-09 09:10:03

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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Frequently Asked Questions

Who is the primary manufacturer of Caplugs/Evergreen?

The registered manufacturer of record for Caplugs/Evergreen is CAPlugs.

What is the Primary UDI-DI identifier for Caplugs/Evergreen?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 230-1092-Y3K.

What classification code is assigned to this device?

This device is registered under product classification code JQW.

Similar Classification Devices (JQW)

Other Devices by CAPlugs

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