gudid
Primary ID: 1
Dentemp (UDI 1)
Manufactured by Doc Brands, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dentemp - Primary ID 1
Device Regulatory Overview
The Dentemp (Model/Catalog Number: 1) is a medical device manufactured by Doc Brands, Inc.. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- EMA
- Device Name
- Dentemp is composed of zinc oxide-eugenol and intended as an over the counter temporary dental cement for re-cementing loose caps or crowns and replacing lost fillings.
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
🔒 Token Gated
{
"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 Dentemp?
The registered manufacturer of record for Dentemp is Doc Brands, Inc..
What is the Primary UDI-DI identifier for Dentemp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code EMA.
Similar Classification Devices (EMA)
Other Devices by Doc Brands, Inc.
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