gudid
Primary ID: UROT1041
Medline (UDI UROT1041)
Manufactured by MEDLINE INDUSTRIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medline - Primary ID UROT1041
Device Regulatory Overview
The Medline (Model/Catalog Number: UROT1041) is a medical device manufactured by MEDLINE INDUSTRIES, INC.. This product is indexed under FDA Product Code / Category Classification OHR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UROT1041
- Product Code / EMDN
- OHR
- Device Name
- TRAY CAUTI TEMP SENS 16FR 10ML
- Database Sync Date
- 2026-08-09 09:15:46
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 Medline?
The registered manufacturer of record for Medline is MEDLINE INDUSTRIES, INC..
What is the Primary UDI-DI identifier for Medline?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UROT1041.
What classification code is assigned to this device?
This device is registered under product classification code OHR.
Similar Classification Devices (OHR)
Other Devices by MEDLINE INDUSTRIES, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint