gudid
Primary ID: 989767
Honigum Pro (UDI 989767)
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 Pro - Primary ID 989767
Device Regulatory Overview
The Honigum Pro (Model/Catalog Number: 989767) 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
- 989767
- Product Code / EMDN
- ELW
- Device Name
- VPS-based impression material. Heavy-bodied and light-bodied consistency. Impression made your way. Content: 2 cartridges Honigum Pro-Heavy @ 50 ml paste, 1 cartridge Honigum Pro-Light @ 50 ml paste, accessories.
- Database Sync Date
- 2026-08-09 09:23:50
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Honigum Pro?
The registered manufacturer of record for Honigum Pro is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Honigum Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 989767.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint