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

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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

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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

UDI-DI variants

37 UDI-DI variants

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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

6272MA-AR24000104262556377074
8033MA-AR24000104262556376909
12676-AR23URG0104262556376954
9184A-AR24000104262556376831
6276MA-AR24000104262556377104
12676-AR24000104262556376947
9184A-AR24000404262556376824
12649-AR23URG0104262556376923
9104MA-AR24000104262556377036
12675-AR23URG0104262556376978
6247MA-AR840000104262556377012
7266MA-AR240000104262556377111

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