gudid
Primary ID: 799517
KOLORZ (UDI 799517)
Manufactured by DMG AMERICA, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KOLORZ - Primary ID 799517
Device Regulatory Overview
The KOLORZ (Model/Catalog Number: 799517) is a medical device manufactured by DMG AMERICA, LLC. This product is indexed under FDA Product Code / Category Classification LBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 799517
- Product Code / EMDN
- LBH
- Device Name
- KOLORZ CLEARSHIELD 5% NAF VARNISH WHITE CARAMEL 200 PACK
- Database Sync Date
- 2026-08-09 09:02:02
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 KOLORZ?
The registered manufacturer of record for KOLORZ is DMG AMERICA, LLC.
What is the Primary UDI-DI identifier for KOLORZ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 799517.
What classification code is assigned to this device?
This device is registered under product classification code LBH.
Similar Classification Devices (LBH)
Other Devices by DMG AMERICA, LLC
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