TRY-ME DENTASOAK KIT (UDI 235-024)
Manufactured by Great Lakes Dental Technologies, Ltd.
Device Regulatory Overview
The TRY-ME DENTASOAK KIT (Model/Catalog Number: 235-024) is a medical device manufactured by Great Lakes Dental Technologies, Ltd.. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 235-024
- Product Code / EMDN
- EFT
- Device Name
- TRY-ME DENTASOAK KIT
- 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 TRY-ME DENTASOAK KIT?
The registered manufacturer of record for TRY-ME DENTASOAK KIT is Great Lakes Dental Technologies, Ltd..
What is the Primary UDI-DI identifier for TRY-ME DENTASOAK KIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 235-024.
What classification code is assigned to this device?
This device is registered under product classification code EFT.
Similar Classification Devices (EFT)
Other Devices by Great Lakes Dental Technologies, Ltd.
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