eudamed_udi
Primary ID: 05051986008356
3x95 Cannula + Luer (UDI 05051986008356)
Manufactured by Surgical Innovations Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 3x95 Cannula + Luer - Primary ID 05051986008356
Device Regulatory Overview
The 3x95 Cannula + Luer (Model/Catalog Number: YC0309501) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L1207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- YC0309501
- Product Code / EMDN
- L1207
- Device Name
- 3x95 Cannula + Luer
- Database Sync Date
- 2026-08-09 16:47:17
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 3x95 Cannula + Luer?
The registered manufacturer of record for 3x95 Cannula + Luer is Surgical Innovations Ltd..
What is the Primary UDI-DI identifier for 3x95 Cannula + Luer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986008356.
What classification code is assigned to this device?
This device is registered under product classification code L1207.
Similar Classification Devices (L1207)
Other Devices by Surgical Innovations Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint