gudid Primary ID: 8.000.4981

DEXIS IXS S1 Kit (UDI 8.000.4981)

Manufactured by Dental Imaging Technologies Corporation

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DEXIS IXS S1 Kit (Model/Catalog Number: 8.000.4981) is a medical device manufactured by Dental Imaging Technologies Corporation. This product is indexed under FDA Product Code / Category Classification MUH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8.000.4981
Product Code / EMDN: MUH
Device Name
Database Sync Date: 2026-08-09 09:01:55

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of DEXIS IXS S1 Kit?

The registered manufacturer of record for DEXIS IXS S1 Kit is Dental Imaging Technologies Corporation.

What is the Primary UDI-DI identifier for DEXIS IXS S1 Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8.000.4981.

What classification code is assigned to this device?

This device is registered under product classification code MUH.

Similar Classification Devices (MUH)

Other Devices by Dental Imaging Technologies Corporation

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint