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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 — 12 UDI-DI variants, MDR (Gimmi GmbH)

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Surgical Instrument

4049047LGZ03ANA27DRO6S

12 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: 4049047LGZ03ANA27DRO6S
Device name: Surgical Instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSPTNZ75Q7JAS0643ZHX5864

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

WI.1361.1504049047779575
WI.1353.1404049047779537
WI.1351.1104049047779513
WI.1358.1204049047779551
WI.1352.1404049047779520
WI.1364.1504049047779599
WI.1358.1304049047779568
WI.1377.1504049047655282
WI.1357.1204049047779544
WI.1376.1004049047110392
WI.1350.1304049047110323
WI.1362.1504049047779582