Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Surgical Instrument — 33 UDI-DI variants, MDR (Gimmi GmbH)

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Surgical Instrument

4049047LDW03ANA27DROYB

33 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4049047LDW03ANA27DROYB
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

33 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSN0D342MZJK8A0FPT6AD497

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.1447.0104049047025436
AQ.1451.0104049047692805
AQ.1447.5004049047025542
AQ.1448.0004049047025566
AQ.1447.6004049047025559
AQ.1449.0404049047025610
AQ.1447.0604049047025481
AQ.1450.2104049047692775
AQ.1447.8004049047692676
AQ.1451.0004049047692799
AQ.1450.0004049047025641
AQ.1447.1204049047025535
AQ.1449.0204049047025597
AQ.1450.5004049047692782
AQ.1448.4104049047692706
AQ.1448.4004049047692690
AQ.1448.0104049047692683
AQ.1447.0504049047025474
AQ.1449.0304049047025603
AQ.1449.0104049047025580
AQ.1448.4204049047692713
AQ.1448.5004049047692744
AQ.1449.1104049047692768
AQ.1447.0304049047025450
AQ.1447.0404049047025467

1 2