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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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Product for cleaning and storage — 135 UDI-DI variants, MDR

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 30, 2026

Product for cleaning and storage

4049047SAC08ABA27DRBEU

135 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4049047SAC08ABA27DRBEU
Device name: Product for cleaning and storage
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

135 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSPYHFHJ4EQ5ABSJM3N165GF

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

R.0152.1004049047081777
R.0180.1004049047651642
R.0147.1004049047515838
R.0457.0004049047085980
R.0455.3404049047651314
R.0452.0204049047085706
R.0176.1004049047082019
R.0253.1004049047082118
R.0545.2204049047086741
R.0545.1004049047086628

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