gudid Primary ID: 500

Caplugs/Evergreen (UDI 500)

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: 500) is a medical device manufactured by CAPlugs. This product is indexed under FDA Product Code / Category Classification LIB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 500
Product Code / EMDN: LIB
Device Name: TEST TUBE 10X75MM
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 500.

What classification code is assigned to this device?

This device is registered under product classification code LIB.

Similar Classification Devices (LIB)

Other Devices by CAPlugs

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