Ionosit Baseliner (UDI 223002)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Device Regulatory Overview
The Ionosit Baseliner (Model/Catalog Number: 223002) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification EBD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 223002
- Product Code / EMDN
- EBD
- Device Name
- Light-curing compomer base liner. Gap-free restorations. Content: 2 syringes @ 1.5 g 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 Ionosit Baseliner?
The registered manufacturer of record for Ionosit Baseliner is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for Ionosit Baseliner?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 223002.
What classification code is assigned to this device?
This device is registered under product classification code EBD.
Similar Classification Devices (EBD)
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