gudid Primary ID: 1348E

3M Attest (UDI 1348E)

Manufactured by 3M COMPANY

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 3M Attest (Model/Catalog Number: 1348E) is a medical device manufactured by 3M COMPANY. This product is indexed under FDA Product Code / Category Classification QKM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1348E
Product Code / EMDN: QKM
Device Name: 3M Attest VH2O2 Tri-Metric Chemical Indicator, 250 each/pouch, 4 pouches/case, 1348E
Database Sync Date: 2026-08-09 09:59:24

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 3M Attest?

The registered manufacturer of record for 3M Attest is 3M COMPANY.

What is the Primary UDI-DI identifier for 3M Attest?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1348E.

What classification code is assigned to this device?

This device is registered under product classification code QKM.

Similar Classification Devices (QKM)

Other Devices by 3M COMPANY

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