gudid
Primary ID: IBNE
Bonded Herbst - RPE (UDI IBNE)
Manufactured by Great Lakes Dental Technologies, Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bonded Herbst - RPE - Primary ID IBNE
Device Regulatory Overview
The Bonded Herbst - RPE (Model/Catalog Number: IBNE) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IBNE
- Product Code / EMDN
- LRK
- Device Name
- Database Sync Date
- 2026-08-09 09:14:54
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 Bonded Herbst - RPE?
The registered manufacturer of record for Bonded Herbst - RPE is Great Lakes Dental Technologies, Ltd..
What is the Primary UDI-DI identifier for Bonded Herbst - RPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IBNE.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Great Lakes Dental Technologies, Ltd.
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