gudid
Primary ID: 00038904806A
Dentek (UDI 00038904806A)
Manufactured by DenTek Oral Care, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dentek - Primary ID 00038904806A
Device Regulatory Overview
The Dentek (Model/Catalog Number: 00038904806A) is a medical device manufactured by DenTek Oral Care, Inc.. This product is indexed under FDA Product Code / Category Classification OLR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00038904806A
- Product Code / EMDN
- OLR
- Device Name
- DNTK CANKER RELIEF 6CT PATCH 24
- Database Sync Date
- 2026-08-09 09:08:50
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 Dentek?
The registered manufacturer of record for Dentek is DenTek Oral Care, Inc..
What is the Primary UDI-DI identifier for Dentek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00038904806A.
What classification code is assigned to this device?
This device is registered under product classification code OLR.
Similar Classification Devices (OLR)
Other Devices by DenTek Oral Care, Inc.
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