GLO MOUTHGUARD PURPLE (DZ) *I (UDI 191-023)
Manufactured by Great Lakes Dental Technologies, Ltd.
Device Regulatory Overview
The GLO MOUTHGUARD PURPLE (DZ) *I (Model/Catalog Number: 191-023) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification DYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 191-023
- Product Code / EMDN
- DYJ
- Device Name
- GLO MOUTHGUARD PURPLE (DZ) *I
- 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 GLO MOUTHGUARD PURPLE (DZ) *I?
The registered manufacturer of record for GLO MOUTHGUARD PURPLE (DZ) *I is Great Lakes Dental Technologies, Ltd..
What is the Primary UDI-DI identifier for GLO MOUTHGUARD PURPLE (DZ) *I?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 191-023.
What classification code is assigned to this device?
This device is registered under product classification code DYJ.
Similar Classification Devices (DYJ)
Other Devices by Great Lakes Dental Technologies, Ltd.
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