eudamed_udi
Primary ID: +G399CTEXD111230F
Explorer (UDI +G399CTEXD111230F)
Manufactured by CROSSTEX (PRIVATE) LIMITED.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Explorer - Primary ID +G399CTEXD111230F
Device Regulatory Overview
The Explorer (Model/Catalog Number: CT-EXD11/123) is a medical device manufactured by CROSSTEX (PRIVATE) LIMITED.. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CT-EXD11/123
- Product Code / EMDN
- L159003
- Device Name
- Explorer
- Database Sync Date
- 2026-08-09 17:10:18
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 Explorer?
The registered manufacturer of record for Explorer is CROSSTEX (PRIVATE) LIMITED..
What is the Primary UDI-DI identifier for Explorer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G399CTEXD111230F.
What classification code is assigned to this device?
This device is registered under product classification code L159003.
Similar Classification Devices (L159003)
Other Devices by CROSSTEX (PRIVATE) LIMITED.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint