gudid
Primary ID: 11210590
BioXmark (UDI 11210590)
Manufactured by MEDTEC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioXmark - Primary ID 11210590
Device Regulatory Overview
The BioXmark (Model/Catalog Number: 11210590) is a medical device manufactured by MEDTEC, INC.. This product is indexed under FDA Product Code / Category Classification QUV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11210590
- Product Code / EMDN
- QUV
- Device Name
- Phase-Changing Fiducial Marker
- Database Sync Date
- 2026-08-09 09:12:36
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 BioXmark?
The registered manufacturer of record for BioXmark is MEDTEC, INC..
What is the Primary UDI-DI identifier for BioXmark?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11210590.
What classification code is assigned to this device?
This device is registered under product classification code QUV.
Similar Classification Devices (QUV)
Other Devices by MEDTEC, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint