GUDIDData
gudid Primary ID: S7005

FOOT PEDAL (UDI S7005)

Manufactured by Stockert GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FOOT PEDAL - Primary ID S7005

Device Regulatory Overview

The FOOT PEDAL (Model/Catalog Number: S7005) is a medical device manufactured by Stockert GmbH. This product is indexed under FDA Product Code / Category Classification DRF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S7005
Product Code / EMDN
DRF
Device Name
Database Sync Date
2026-08-09 09:17:35

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 FOOT PEDAL?

The registered manufacturer of record for FOOT PEDAL is Stockert GmbH.

What is the Primary UDI-DI identifier for FOOT PEDAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S7005.

What classification code is assigned to this device?

This device is registered under product classification code DRF.

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