Banded Herbst-Rpe Remov Lower (UDI IBAER)
Manufactured by Great Lakes Dental Technologies, Ltd.
Device Regulatory Overview
The Banded Herbst-Rpe Remov Lower (Model/Catalog Number: IBAER) 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
- IBAER
- 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 Banded Herbst-Rpe Remov Lower?
The registered manufacturer of record for Banded Herbst-Rpe Remov Lower is Great Lakes Dental Technologies, Ltd..
What is the Primary UDI-DI identifier for Banded Herbst-Rpe Remov Lower?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IBAER.
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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