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

11512-AR24000104262556374905
10071-AR24000104262556375636
11287-AR24000104262556374165
12453_V02-AR24000104262556374028
9330M-AR84000104262556372536
9529M-AR24000104262556374417
10247M-AR84000104262556376817
11435_V02-AR25GLM0104262556370891
11714-AR24000104262556376534
9515M-AR24000104262556372321
10511-AR43TEC0104262556376367
10088M-AR24000104262556372680
11746-AR24000104262556375162
9858M-AR43TEC0104262556374431
12407-AR24000104262556371065
12411_V02-AR25GLM0104262556371140
12424_V02-AR25GLM0104262556373823
8091M-AR24000104262556373052
12461_V02-AR85000104262556373656
12179_V02-AR85MIR0104262556375063
10124-AR24000104262556372000
11294-AR24000104262556374578
7646M-AR24000104262556372147
11861-AR24000104262556376220
9779M-AR24000104262556373007