gudid
Primary ID: 35014
RelyX Temp E (UDI 35014)
Manufactured by 3M Deutschland GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RelyX Temp E - Primary ID 35014
Device Regulatory Overview
The RelyX Temp E (Model/Catalog Number: 35014) is a medical device manufactured by 3M Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification EMB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 35014
- Product Code / EMDN
- EMB
- Device Name
- 3M ESPE RelyX Temp E Zinc Oxide Eugenol Temporary Cement Refill, 35014
- Database Sync Date
- 2026-08-09 09:38:00
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 RelyX Temp E?
The registered manufacturer of record for RelyX Temp E is 3M Deutschland GmbH.
What is the Primary UDI-DI identifier for RelyX Temp E?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 35014.
What classification code is assigned to this device?
This device is registered under product classification code EMB.
Similar Classification Devices (EMB)
Other Devices by 3M Deutschland GmbH
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