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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Morcellator activeCut — 5 UDI-DI variants, MDR

MD Atlas
Active Medical Xcellence GmbH

Data from EUDAMED, last updated May 23, 2026

Morcellator activeCut

4069019activeCut001VB

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Active Medical Xcellence GmbH

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Device characteristics

Active device

Legacy certificates

Certificate number: 111178U2
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SLG PRÜF UND ZERTIFIZIERUNGS GMBH (0494)
Validity: May 7, 2026 → Dec 15, 2030

Identity & classification

Basic UDI-DI: 4069019activeCut001VB
Device name: Morcellator activeCut
Device model: activeCut
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Active Medical Xcellence GmbH
SRN: DE-MF-000049306
Country: Germany
Email: contact@amx-med.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K76QW232P5V4C067NA8ZQKQC

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

110000104069019000025
110000004069019000032
100000004069019000001
100000204069019000018
400-000304069019000049