GUDIDData
eudamed_udi Primary ID: 05051986000008

235mm Cobra (UDI 05051986000008)

Manufactured by Surgical Innovations Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 235mm Cobra - Primary ID 05051986000008

Device Regulatory Overview

The 235mm Cobra (Model/Catalog Number: 101-47039) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L180802 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
101-47039
Product Code / EMDN
L180802
Device Name
235mm Cobra
Database Sync Date
2026-08-09 16:45:08

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of 235mm Cobra?

The registered manufacturer of record for 235mm Cobra is Surgical Innovations Ltd..

What is the Primary UDI-DI identifier for 235mm Cobra?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986000008.

What classification code is assigned to this device?

This device is registered under product classification code L180802.

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