gudid
Primary ID: S270270
Vivid Root MTA (UDI S270270)
Manufactured by PEARSON DENTAL SUPPLIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vivid Root MTA - Primary ID S270270
Device Regulatory Overview
The Vivid Root MTA (Model/Catalog Number: S270270) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S270270
- Product Code / EMDN
- KIF
- Device Name
- 2 x 300mg
- Database Sync Date
- 2026-08-09 09:15:03
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 Vivid Root MTA?
The registered manufacturer of record for Vivid Root MTA is PEARSON DENTAL SUPPLIES, INC..
What is the Primary UDI-DI identifier for Vivid Root MTA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S270270.
What classification code is assigned to this device?
This device is registered under product classification code KIF.
Similar Classification Devices (KIF)
Other Devices by PEARSON DENTAL SUPPLIES, INC.
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