gudid
Primary ID: 2110100003
VistaSoft (UDI 2110100003)
Manufactured by DRR DENTAL SE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VistaSoft - Primary ID 2110100003
Device Regulatory Overview
The VistaSoft (Model/Catalog Number: 2110100003) is a medical device manufactured by DRR DENTAL SE. This product is indexed under FDA Product Code / Category Classification QIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2110100003
- Product Code / EMDN
- QIH
- Device Name
- Dental Imaging Software.
- Database Sync Date
- 2026-08-09 09:07:32
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of VistaSoft?
The registered manufacturer of record for VistaSoft is DRR DENTAL SE.
What is the Primary UDI-DI identifier for VistaSoft?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2110100003.
What classification code is assigned to this device?
This device is registered under product classification code QIH.
Similar Classification Devices (QIH)
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