NA (UDI 00711211)

Manufactured by STERIS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: 00711211) is a medical device manufactured by STERIS. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 00711211
Product Code / EMDN: KGE
Device Name: The Biopsy Forceps Hot is a disposable biopsy forceps used to obtain mucosal tissue samples during endoscopic procedures.
Database Sync Date: 2026-08-09 09:19:09

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 NA?

The registered manufacturer of record for NA is STERIS.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00711211.

What classification code is assigned to this device?

This device is registered under product classification code KGE.

Similar Classification Devices (KGE)

Other Devices by STERIS

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