Honigum Trial Kit (UDI 999500)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Device Regulatory Overview
The Honigum Trial Kit (Model/Catalog Number: 999500) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 999500
- Product Code / EMDN
- ELW
- Device Name
- VPS-based impression material, Heavy-bodied and light-bodied consistency. Professional precision. Content: 2 cartridges Honigum Heavy @ 50 ml paste, 1 cartridge Honigum Light @ 50 ml paste, Accessories
- Database Sync Date
- 2026-08-09 09:23:50
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 Honigum Trial Kit?
The registered manufacturer of record for Honigum Trial Kit is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Honigum Trial Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 999500.
What classification code is assigned to this device?
This device is registered under product classification code ELW.
Similar Classification Devices (ELW)
Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH
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