Honigum Pro Light (UDI 989831)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Device Regulatory Overview
The Honigum Pro Light (Model/Catalog Number: 989831) 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
- 989831
- Product Code / EMDN
- ELW
- Device Name
- Impression material, light-bodied consistency. Impressions made your way. Content: 2 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 Pro Light?
The registered manufacturer of record for Honigum Pro Light is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Honigum Pro Light?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 989831.
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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