gudid
Primary ID: 999830
Honigum Mono (UDI 999830)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Honigum Mono - Primary ID 999830
Device Regulatory Overview
The Honigum Mono (Model/Catalog Number: 999830) 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
- 999830
- Product Code / EMDN
- ELW
- Device Name
- Impression material, medium-bodied consistency. Professional precision. Content: 4 cartridges @ 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 Mono?
The registered manufacturer of record for Honigum Mono is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Honigum Mono?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 999830.
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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