AMSure® RED RUBBER URETHRAL CATHETER (UDI 10704411001867)
Manufactured by Amsino International Inc.
Device Regulatory Overview
The AMSure® RED RUBBER URETHRAL CATHETER (Model/Catalog Number: AS44024) is a medical device manufactured by Amsino International Inc.. This product is indexed under FDA Product Code / Category Classification U01010502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AS44024
- Product Code / EMDN
- U01010502
- Device Name
- Urethral Catheter
- Database Sync Date
- 2026-08-09 16:28:49
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 AMSure® RED RUBBER URETHRAL CATHETER?
The registered manufacturer of record for AMSure® RED RUBBER URETHRAL CATHETER is Amsino International Inc..
What is the Primary UDI-DI identifier for AMSure® RED RUBBER URETHRAL CATHETER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10704411001867.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by Amsino International Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint