eudamed_udi Primary ID: 05051986000091

305mm Long Fenestrated Grasper (UDI 05051986000091)

Manufactured by Surgical Innovations Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The 305mm Long Fenestrated Grasper (Model/Catalog Number: 101-48021) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L1899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 101-48021
Product Code / EMDN: L1899
Device Name: 305mm Long Fenestrated Grasper
Database Sync Date: 2026-08-09 16:58:35

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 305mm Long Fenestrated Grasper?

The registered manufacturer of record for 305mm Long Fenestrated Grasper is Surgical Innovations Ltd..

What is the Primary UDI-DI identifier for 305mm Long Fenestrated Grasper?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986000091.

What classification code is assigned to this device?

This device is registered under product classification code L1899.

Similar Classification Devices (L1899)

Other Devices by Surgical Innovations Ltd.

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