gudid
Primary ID: 1
Apex Capture Software (UDI 1)
Manufactured by MASTERLINK LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Apex Capture Software - Primary ID 1
Device Regulatory Overview
The Apex Capture Software (Model/Catalog Number: 1) is a medical device manufactured by MASTERLINK LLC. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- LLZ
- Device Name
- Dental imaging capture, enhance and display software.
- Database Sync Date
- 2026-08-09 09:03:36
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 Apex Capture Software?
The registered manufacturer of record for Apex Capture Software is MASTERLINK LLC.
What is the Primary UDI-DI identifier for Apex Capture Software?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code LLZ.
Similar Classification Devices (LLZ)
Other Devices by MASTERLINK LLC
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