gudid
Primary ID: 502450
CHX (UDI 502450)
Manufactured by Vista Dental
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHX - Primary ID 502450
Device Regulatory Overview
The CHX (Model/Catalog Number: 502450) is a medical device manufactured by Vista Dental. This product is indexed under FDA Product Code / Category Classification KJJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 502450
- Product Code / EMDN
- KJJ
- Device Name
- 2% Chlorhexidine Gluconate - use prior to restorative preparations of crowns and composites. Restorative kit includes (4) 1.2ml prefilled syringes & 40 Sol-u-Flo tips.
- Database Sync Date
- 2026-08-09 09:46:37
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 CHX?
The registered manufacturer of record for CHX is Vista Dental.
What is the Primary UDI-DI identifier for CHX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 502450.
What classification code is assigned to this device?
This device is registered under product classification code KJJ.
Similar Classification Devices (KJJ)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint