eudamed_udi
Primary ID: 08902095300411
Rectal Catheter (UDI 08902095300411)
Manufactured by Poly Medicure Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rectal Catheter - Primary ID 08902095300411
Device Regulatory Overview
The Rectal Catheter (Model/Catalog Number: 30041) is a medical device manufactured by Poly Medicure Limited. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30041
- Product Code / EMDN
- G020301
- Device Name
- Rectal Catheter
- Database Sync Date
- 2026-08-09 16:46:49
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 Rectal Catheter?
The registered manufacturer of record for Rectal Catheter is Poly Medicure Limited.
What is the Primary UDI-DI identifier for Rectal Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08902095300411.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Poly Medicure Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint