gudid
Primary ID: 906101
Enamelize (UDI 906101)
Manufactured by DeltaMed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Enamelize - Primary ID 906101
Device Regulatory Overview
The Enamelize (Model/Catalog Number: 906101) is a medical device manufactured by DeltaMed GmbH. This product is indexed under FDA Product Code / Category Classification EJR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 906101
- Product Code / EMDN
- EJR
- Device Name
- Enamelize, Tube 36g
- Database Sync Date
- 2026-08-09 09:05:54
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 Enamelize?
The registered manufacturer of record for Enamelize is DeltaMed GmbH.
What is the Primary UDI-DI identifier for Enamelize?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 906101.
What classification code is assigned to this device?
This device is registered under product classification code EJR.
Similar Classification Devices (EJR)
Other Devices by DeltaMed GmbH
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