eudamed_udi Primary ID: 04049203003094

Forceps, Grasping, Flexible Endoscopic (UDI 04049203003094)

Manufactured by STEMA Medizintechnik GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Forceps, Grasping, Flexible Endoscopic (Model/Catalog Number: AC-009-212) is a medical device manufactured by STEMA Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification L060403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AC-009-212
Product Code / EMDN: L060403
Device Name: Forceps, Grasping, Flexible Endoscopic
Database Sync Date: 2026-08-09 16:46:20

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 Forceps, Grasping, Flexible Endoscopic?

The registered manufacturer of record for Forceps, Grasping, Flexible Endoscopic is STEMA Medizintechnik GmbH.

What is the Primary UDI-DI identifier for Forceps, Grasping, Flexible Endoscopic?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049203003094.

What classification code is assigned to this device?

This device is registered under product classification code L060403.

Similar Classification Devices (L060403)

Other Devices by STEMA Medizintechnik GmbH

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