gudid
Primary ID: 999539
Honigum Light (UDI 999539)
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 Light - Primary ID 999539
Device Regulatory Overview
The Honigum Light (Model/Catalog Number: 999539) 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
- 999539
- Product Code / EMDN
- ELW
- Device Name
- Impression material, light-bodied consistency. Professional precision. Content: 4 cartridges @ 25 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 Light?
The registered manufacturer of record for Honigum Light is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Honigum Light?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 999539.
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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