gudid Primary ID: CVS TRUEplus lancets - 33G

TRUEplus (UDI CVS TRUEplus lancets - 33G)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TRUEplus (Model/Catalog Number: CVS TRUEplus lancets - 33G) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification QRK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CVS TRUEplus lancets - 33G
Product Code / EMDN: QRK
Device Name: CVS lancets - 33G 100ct
Database Sync Date: 2026-08-09 09:08:49

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 TRUEplus?

The registered manufacturer of record for TRUEplus is TRIVIDIA HEALTH, INC..

What is the Primary UDI-DI identifier for TRUEplus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CVS TRUEplus lancets - 33G.

What classification code is assigned to this device?

This device is registered under product classification code QRK.

Similar Classification Devices (QRK)

Other Devices by TRIVIDIA HEALTH, INC.

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