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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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Sheaths — 19 UDI-DI variants, MDR (Gimmi GmbH)

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Sheaths

4049047AAD10BIA27DREQB

19 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: 4049047AAD10BIA27DREQB
Device name: Sheaths
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

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMR4J5WS92EDH4T24MFBYP7

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.9696.0204049047785323
T.9042.5204049047106579
T.9056.8004049047672760
T.9049.1704049047106661
T.9042.5304049047106586
T.9695.1404049047785255
T.9042.5404049047106593
T.9636.0104049047788157
T.9665.0204049047787709
T.9042.5104049047106562
T.9049.1904049047106678
T.9696.1104049047797883
T.9042.5004049047106555
T.9665.0404049047787716
T.9049.2304049047106692
T.9049.2504049047106708
T.9695.0504049047785163
T.9049.2104049047106685
T.9637.0104049047788218