gudid Primary ID: AR-S9800-F2

Sutter (UDI AR-S9800-F2)

Manufactured by Sutter Medizintechnik GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Sutter (Model/Catalog Number: AR-S9800-F2) is a medical device manufactured by Sutter Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2744-2020 View Full Alert →

Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps are provided with ba...

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Technical Specifications

Model Number: AR-S9800-F2
Product Code / EMDN: GEI
Device Name: Foot-switch, 2 pedals small Arthrex explosion proof, 4m cable Class IPX8
Database Sync Date: 2026-08-09 09:51:21

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 Sutter?

The registered manufacturer of record for Sutter is Sutter Medizintechnik GmbH.

What is the Primary UDI-DI identifier for Sutter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AR-S9800-F2.

What classification code is assigned to this device?

This device is registered under product classification code GEI.

Similar Classification Devices (GEI)

Other Devices by Sutter Medizintechnik GmbH

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