gudid
Primary ID: ZOER-RF
Zoer Reinforced (UDI ZOER-RF)
Manufactured by D.S.I DENTAL SOLUTIONS LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zoer Reinforced - Primary ID ZOER-RF
Device Regulatory Overview
The Zoer Reinforced (Model/Catalog Number: ZOER-RF) is a medical device manufactured by D.S.I DENTAL SOLUTIONS LTD. This product is indexed under FDA Product Code / Category Classification EMB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZOER-RF
- Product Code / EMDN
- EMB
- Device Name
- Database Sync Date
- 2026-08-09 09:01:11
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 Zoer Reinforced?
The registered manufacturer of record for Zoer Reinforced is D.S.I DENTAL SOLUTIONS LTD.
What is the Primary UDI-DI identifier for Zoer Reinforced?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZOER-RF.
What classification code is assigned to this device?
This device is registered under product classification code EMB.
Similar Classification Devices (EMB)
Other Devices by D.S.I DENTAL SOLUTIONS LTD
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