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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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Monopolar & Bipolar Resectoscope — 15 UDI-DI variants, MDR

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Monopolar & Bipolar Resectoscope

4049047AAD10CBA27DREM7

15 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Gimmi GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4049047AAD10CBA27DREM7
Device name: Monopolar & Bipolar Resectoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Gimmi GmbH
SRN: DE-MF-000005445
Country: Germany
Email: QM-RA@gimmi.de
Phone: +49 7461 96590 0

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMRGN37NBA89J4PA8PV0A5X

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

T.9560.2304049047784135
T.9570.1304049047784548
T.9560.2404049047784142
T.9560.1304049047784074
T.9680.1304049047785057
T.9670.1304049047784906
T.9570.1204049047784531
T.9560.1504049047784098
T.9695.0304049047785149
T.9560.2204049047784128
T.9560.1404049047784081
T.9670.1404049047784913
T.9670.1204049047784890
T.9560.1204049047784067
T.9560.2504049047784159