gudid
Primary ID: Z060318
Vivid Etch 40% refill (UDI Z060318)
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 Etch 40% refill - Primary ID Z060318
Device Regulatory Overview
The Vivid Etch 40% refill (Model/Catalog Number: Z060318) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification KLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Z060318
- Product Code / EMDN
- KLE
- Device Name
- 60G
- 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 Etch 40% refill?
The registered manufacturer of record for Vivid Etch 40% refill is PEARSON DENTAL SUPPLIES, INC..
What is the Primary UDI-DI identifier for Vivid Etch 40% refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z060318.
What classification code is assigned to this device?
This device is registered under product classification code KLE.
Similar Classification Devices (KLE)
Other Devices by PEARSON DENTAL SUPPLIES, INC.
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