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

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Surgical Instrument

4049047LDR03ANA27DROTG

93 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: 4049047LDR03ANA27DROTG
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

93 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSN0CPSFB71QP1ZMHKY1X37B

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

QS.1605.0204049047119302
QS.1607.0204049047119494
QO.1009.0304049047075561
QS.1595.0104049047119388
QO.1011.0404049047075653
QS.1597.1404049047716952
QO.1015.0704049047075899
QO.1002.1304049047075271
QS.1605.0804049047387923
QS.1614.1404049047717089
QO.1015.1304049047075905
QO.1002.0404049047075226
QS.1600.0104049047080947
QS.1604.0104049047081005
QS.1595.0604049047716938
QS.1601.2904049047716983
QS.1608.5304049047717058
QS.1608.0404049047120063

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