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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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Saugkompressen, unsteril — 4 UDI-DI variants, MDR (Fuhrmann GmbH)

MD Atlas
Fuhrmann GmbH

Data from EUDAMED, last updated May 23, 2026

Saugkompressen, unsteril

40548580111V1401LC

4 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: Fuhrmann GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40548580111V1401LC
Device name: Saugkompressen, unsteril
Device model: Saugkompressen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Fuhrmann GmbH
SRN: DE-MF-000006652
Country: Germany
Email: info@fuhrmann.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K97JF16S7N5BD3603FE6F4VD

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

Absorbent pads with covering 10 x 10 cm, non-sterile04054858300283
Absorbent pads with covering 10 x 20 cm, non-sterile04054858300306
Absorbent pads with covering 20 x 20 cm, non-sterile04054858300344
Absorbent pads with covering 20 x 40 cm, non-sterile04054858300320