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.

SPATULA — 37 UDI-DI variants, MDR (Remy & Geiser GmbH)

MD Atlas
Remy & Geiser GmbH

Data from EUDAMED, last updated May 23, 2026

SPATULA

426255637SPATULAUZ

37 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?

UDI-DI variants

37 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

basicUdiUlid01KRXTY2CZ8S9AGP9GKT23R43H

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

6255MA-AR84000104262556377050
12675-AR24000104262556376961
9135MA-AR24000104262556376893
6277MA-AR24000104262556377142
11394-AR24000104262556376862
12636-AR23URG0104262556377173
9080MA-AR24000104262556377135
7709MA-AR24000104262556377005
12068-AR24000104262556377166
6257M-AR24000104262556376916
6274MA-AR24000104262556377081
6278MA-AR24000104262556377159
9183-AR24000404262556376848
8629MA-AR24000104262556376992
9906MA-AR84ESP0104262556377098
12649-AR24000104262556376930
10164MA-AR24000104262556376855
12636-AR24000104262556377180
6250MA-AR24000104262556377043
8997MA-AR24000104262556376886
6258MA-AR24000104262556377067
10519MA-AR24000104262556376879
6249MA-AR24000104262556377029
7895MA-AR24000104262556376985
7266MA-AR84000104262556377128

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426255637SPATULAUZ
Device name: SPATULA
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