GUDIDData
gudid Primary ID: 8.000.4980

DEXIS Ti2 Sensor & Acc. Kit - D (UDI 8.000.4980)

Manufactured by Dental Imaging Technologies Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DEXIS Ti2 Sensor & Acc. Kit - D - Primary ID 8.000.4980

Device Regulatory Overview

The DEXIS Ti2 Sensor & Acc. Kit - D (Model/Catalog Number: 8.000.4980) 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
8.000.4980
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 Ti2 Sensor & Acc. Kit - D?

The registered manufacturer of record for DEXIS Ti2 Sensor & Acc. Kit - D is Dental Imaging Technologies Corporation.

What is the Primary UDI-DI identifier for DEXIS Ti2 Sensor & Acc. Kit - D?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8.000.4980.

What classification code is assigned to this device?

This device is registered under product classification code MUH.

Programmatic Export

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

JSON API Endpoint