GUDIDData
eudamed_udi Primary ID: 05060417200054

Crocodile Forceps 5mm (UDI 05060417200054)

Manufactured by Sheffmed Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Crocodile Forceps 5mm - Primary ID 05060417200054

Device Regulatory Overview

The Crocodile Forceps 5mm (Model/Catalog Number: TE11-241S) is a medical device manufactured by Sheffmed Limited. This product is indexed under FDA Product Code / Category Classification Q0399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TE11-241S
Product Code / EMDN
Q0399
Device Name
Forceps - Sterile
Database Sync Date
2026-08-09 16:52:01

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Crocodile Forceps 5mm?

The registered manufacturer of record for Crocodile Forceps 5mm is Sheffmed Limited.

What is the Primary UDI-DI identifier for Crocodile Forceps 5mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060417200054.

What classification code is assigned to this device?

This device is registered under product classification code Q0399.

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