eudamed_udi Primary ID: ESUM780272SG0

Unspecified Brand (UDI ESUM780272SG0)

Manufactured by Sutter Medizintechnik GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 780272SG) is a medical device manufactured by Sutter Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification L180401 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: 780272SG
Product Code / EMDN: L180401
Device Name: Bipolar Forceps
Database Sync Date: 2026-08-09 16:29:09

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 Unspecified Brand?

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

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ESUM780272SG0.

What classification code is assigned to this device?

This device is registered under product classification code L180401.

Similar Classification Devices (L180401)

Other Devices by Sutter Medizintechnik GmbH

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