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

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Surgical Instrument

4049047LFF03ANA27DROJ6

63 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: 4049047LFF03ANA27DROJ6
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

63 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSPN39WNAASPZW5K13M6W92C

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

AQ.1585.1104049047692959
QT.0300.1404049047373339
AQ.1585.1304049047692966
QT.0314.1404049047374831
QT.0304.0204049047378846
QS.1941.1404049047717256
QT.0312.0104049047385424
QT.0314.0204049047374855
QT.0306.0704049047373285
QT.0314.0504049047374879
QT.0312.0304049047385448
AQ.1585.0904049047692942
QT.0314.0404049047374886

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