gudid
Primary ID: DIACEM TEMPNE 3g(Type S)
DIACEM TEMPNE (UDI DIACEM TEMPNE 3g(Type S))
Manufactured by DiaDent Group International
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIACEM TEMPNE - Primary ID DIACEM TEMPNE 3g(Type S)
Device Regulatory Overview
The DIACEM TEMPNE (Model/Catalog Number: DIACEM TEMPNE 3g(Type S)) is a medical device manufactured by DiaDent Group International. This product is indexed under FDA Product Code / Category Classification EMB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DIACEM TEMPNE 3g(Type S)
- Product Code / EMDN
- EMB
- Device Name
- This product is a non-eugenol type dental adhesive cement that corresponds to type 1 (for temporary cementation) according to the classification of ISO3107. Zinc oxide reacts with 2-ethoxybenzoic acid to have relatively low adhesion and strength and is used for temporary bonding.
- Database Sync Date
- 2026-08-09 09:56:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DIACEM TEMPNE?
The registered manufacturer of record for DIACEM TEMPNE is DiaDent Group International.
What is the Primary UDI-DI identifier for DIACEM TEMPNE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DIACEM TEMPNE 3g(Type S).
What classification code is assigned to this device?
This device is registered under product classification code EMB.
Similar Classification Devices (EMB)
Other Devices by DiaDent Group International
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint