gudid Primary ID: T3018-7033

Sure-Vue (UDI T3018-7033)

Manufactured by FISHER SCIENTIFIC COMPANY L.L.C.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Sure-Vue (Model/Catalog Number: T3018-7033) is a medical device manufactured by FISHER SCIENTIFIC COMPANY L.L.C.. This product is indexed under FDA Product Code / Category Classification DHR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: T3018-7033
Product Code / EMDN: DHR
Device Name: SURE-VUE RF 100TEST/PK
Database Sync Date: 2026-08-09 09:00:34

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 Sure-Vue?

The registered manufacturer of record for Sure-Vue is FISHER SCIENTIFIC COMPANY L.L.C..

What is the Primary UDI-DI identifier for Sure-Vue?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is T3018-7033.

What classification code is assigned to this device?

This device is registered under product classification code DHR.

Similar Classification Devices (DHR)

Other Devices by FISHER SCIENTIFIC COMPANY L.L.C.

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