gudid
Primary ID: 1100-100
Turbo-CR (UDI 1100-100)
Manufactured by ESSENTIAL DENTAL SYSTEMS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Turbo-CR - Primary ID 1100-100
Device Regulatory Overview
The Turbo-CR (Model/Catalog Number: 1100-100) is a medical device manufactured by ESSENTIAL DENTAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification KMT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1100-100
- Product Code / EMDN
- KMT
- Device Name
- Disposable Fluoride Trays
- Database Sync Date
- 2026-08-09 09:41:29
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 Turbo-CR?
The registered manufacturer of record for Turbo-CR is ESSENTIAL DENTAL SYSTEMS, INC..
What is the Primary UDI-DI identifier for Turbo-CR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1100-100.
What classification code is assigned to this device?
This device is registered under product classification code KMT.
Similar Classification Devices (KMT)
Other Devices by ESSENTIAL DENTAL SYSTEMS, INC.
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