gudid
Primary ID: 12x1 case
Detojet (UDI 12x1 case)
Manufactured by ALCONOX INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Detojet - Primary ID 12x1 case
Device Regulatory Overview
The Detojet (Model/Catalog Number: 12x1 case) is a medical device manufactured by ALCONOX INC. This product is indexed under FDA Product Code / Category Classification FLG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12x1 case
- Product Code / EMDN
- FLG
- Device Name
- Cleaner for ultrasonic cleaning of medical devices
- Database Sync Date
- 2026-08-09 09:17:29
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 Detojet?
The registered manufacturer of record for Detojet is ALCONOX INC.
What is the Primary UDI-DI identifier for Detojet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12x1 case.
What classification code is assigned to this device?
This device is registered under product classification code FLG.
Similar Classification Devices (FLG)
Other Devices by ALCONOX INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint