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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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Surgical Instrument — 14 UDI-DI variants, MDR (Gimmi GmbH)

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Surgical Instrument

4049047LCR03ANA27DROSB

14 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: 4049047LCR03ANA27DROSB
Device name: Surgical Instrument
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

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSN0C7886013395B8N9PKWKM

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

KO.1609.0104049047061854
KO.1159.0004049047061809
KO.1186.0104049047708841
KO.1614.1004049047709145
KO.1155.1104049047658498
KO.1186.0004049047708834
KO.1170.0004049047708803
KO.1171.0004049047708827
KO.1614.0104049047061861
KO.1162.0104049047708797
KO.1300.0404049047708896
KO.1170.0104049047708810
KO.1609.0004049047061847
KO.1155.0904049047061793