GUDIDData
eudamed_udi Primary ID: 05051986000176

355mm Duckbill Forceps (UDI 05051986000176)

Manufactured by Surgical Innovations Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 355mm Duckbill Forceps - Primary ID 05051986000176

Device Regulatory Overview

The 355mm Duckbill Forceps (Model/Catalog Number: 101-49032) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L180402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
101-49032
Product Code / EMDN
L180402
Device Name
355mm Duckbill Forceps
Database Sync Date
2026-08-09 16:51:40

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 355mm Duckbill Forceps?

The registered manufacturer of record for 355mm Duckbill Forceps is Surgical Innovations Ltd..

What is the Primary UDI-DI identifier for 355mm Duckbill Forceps?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986000176.

What classification code is assigned to this device?

This device is registered under product classification code L180402.

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