VeriSuite (UDI 1.8)
Manufactured by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH
Device Regulatory Overview
The VeriSuite (Model/Catalog Number: 1.8) is a medical device manufactured by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.8
- Product Code / EMDN
- LHN
- Device Name
- Database Sync Date
- 2026-08-09 09:53:22
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 VeriSuite?
The registered manufacturer of record for VeriSuite is MedCom Gesellschaft fr medizinische Bildverarbeitung mbH.
What is the Primary UDI-DI identifier for VeriSuite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.8.
What classification code is assigned to this device?
This device is registered under product classification code LHN.
Similar Classification Devices (LHN)
Other Devices by MedCom Gesellschaft fr medizinische Bildverarbeitung mbH
Programmatic Export
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JSON API Endpoint