Kukident (UDI 08006540747506)
Manufactured by Procter & Gamble Technical Centres Limited
Device Regulatory Overview
The Kukident (Model/Catalog Number: 80718393) is a medical device manufactured by Procter & Gamble Technical Centres Limited. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80718393
- Product Code / EMDN
- Q010280
- Device Name
- Denture Adhesive
- Database Sync Date
- 2026-08-09 16:51:04
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 Kukident?
The registered manufacturer of record for Kukident is Procter & Gamble Technical Centres Limited.
What is the Primary UDI-DI identifier for Kukident?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08006540747506.
What classification code is assigned to this device?
This device is registered under product classification code Q010280.
Similar Classification Devices (Q010280)
Other Devices by Procter & Gamble Technical Centres Limited
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