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.

DROPPER ASSEMBLY — 609 UDI-DI variants, MDR (Remy & Geiser GmbH)

MD Atlas
Remy & Geiser GmbH

Data from EUDAMED, last updated May 23, 2026

DROPPER ASSEMBLY

426255637PIPETTETA

609 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: Remy & Geiser 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: 426255637PIPETTETA
Device name: DROPPER ASSEMBLY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Remy & Geiser GmbH
SRN: DE-MF-000020726
Country: Germany
Email: conny.schneider.heinze@gerresheimer.com
Phone: +49 171 5276399

Variants by status

UDI-DI variants

609 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

basicUdiUlid01KRXHAB481VAZDYA31Q9TDX3E

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

11737-AR24000104262556373298
11478-AR24000104262556375407
6382M-AR24000104262556372994
12426_V02-AR25GLM0104262556373878
9743M-AR84ESP0104262556372291
8879M-AR840000104262556372079
7490M-AR24000104262556372550
10128M-AR24000104262556372154
12460_V02-AR85000104262556373670
10783-AR24000104262556374622
10102M-AR24000104262556372574
11490-AR24000104262556375551
11766-AR24000104262556373762
6488-AR84000104262556373199
11360-AR24000104262556372932
11765-AR84000104262556370952
8559M-AR42000104262556375001
11747-AR24000104262556375179
10958-AR240000104262556370785
9693-AR24000104262556375599
10958_V02-AR85000104262556370778
11996-AR24000104262556373731
6044-AR24000104262556371843
10760-AR85MIR0104262556374394
12462-AR2400104262556373694