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.

Laryngoscope, Otoscope and Accessories — 102 UDI-DI variants, MDR

MD Atlas
Gimmi GmbH

Data from EUDAMED, last updated May 31, 2026

Laryngoscope, Otoscope and Accessories

4049047ZAJ03AFA27DROVX

102 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4049047ZAJ03AFA27DROVX
Device name: Laryngoscope, Otoscope and Accessories
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

102 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

basicUdiUlid01KSQ0YDK4ESST23NF59FBEKEJ

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

QL.3000.0104049047224822
QL.3007.0104049047224884
AV.1571.1004049047693567
AV.1630.0104049047160700
AV.1571.0404049047027485
AV.1551.0004049047693468
AV.1350.0204049047693048
AV.1383.0204049047693147
AV.1670.0104049047693703
QL.3001.0204049047714576
AV.1384.0504049047693208
AV.1390.0404049047027256
AV.1389.0204049047693291
QL.3001.0404049047714590
QL.3006.0204049047714668
AV.1551.0104049047027379
QL.3002.0204049047628743
QL.3002.0104049047628736
AV.1356.2004049047693123
AV.1356.0204049047027065
AV.1581.1004049047693642
QL.3002.0304049047628750
AV.1550.0104049047693437
AV.1417.0004049047693321
QL.3000.0204049047224785

1 2 3 4 5