GUDIDData
eudamed_udi Primary ID: 05056111309223

Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel (UDI 05056111309223)

Manufactured by Surtex Instruments Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel - Primary ID 05056111309223

Device Regulatory Overview

The Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel (Model/Catalog Number: NS-324-01 T) is a medical device manufactured by Surtex Instruments Ltd. This product is indexed under FDA Product Code / Category Classification L091302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NS-324-01 T
Product Code / EMDN
L091302
Device Name
Cutting Instruments
Database Sync Date
2026-08-09 16:28:46

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 Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel?

The registered manufacturer of record for Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel is Surtex Instruments Ltd.

What is the Primary UDI-DI identifier for Ferris-Smith Kerrison Punch With Thin Footplate Detachable Model - Up Cutting 20 cm - 8" Bite Size 1 mm Stainless Steel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056111309223.

What classification code is assigned to this device?

This device is registered under product classification code L091302.

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