gudid
Primary ID: 10.309.072
DENFINITY (UDI 10.309.072)
Manufactured by 3R - INDUSTRIA E COMERCIO EIRELI
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DENFINITY - Primary ID 10.309.072
Device Regulatory Overview
The DENFINITY (Model/Catalog Number: 10.309.072) is a medical device manufactured by 3R - INDUSTRIA E COMERCIO EIRELI. This product is indexed under FDA Product Code / Category Classification EHM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10.309.072
- Product Code / EMDN
- EHM
- Device Name
- Diamond Finishing & Polishing Strips 4.00mm Medium 10 Pk
- Database Sync Date
- 2026-08-09 09:05:13
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 DENFINITY?
The registered manufacturer of record for DENFINITY is 3R - INDUSTRIA E COMERCIO EIRELI.
What is the Primary UDI-DI identifier for DENFINITY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10.309.072.
What classification code is assigned to this device?
This device is registered under product classification code EHM.
Similar Classification Devices (EHM)
Other Devices by 3R - INDUSTRIA E COMERCIO EIRELI
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