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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, EO steril — 4 UDI-DI variants, MDR (Fuhrmann GmbH)

MD Atlas
Fuhrmann GmbH

Data from EUDAMED, last updated May 23, 2026

Saugkompressen, EO steril

40548580122V1401MA

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: 40548580122V1401MA
Device name: Saugkompressen, EO steril
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

basicUdiUlid01K97MC0DR6YC70C0460Y1NT7P

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 Pad with covering, 10 x 10 cm, á 1, sterile04054858030166
Absorbent Pad with covering, 10 x 20 cm, á 1, sterile04054858030159
Absorbent Pad with covering, 20 x 20 cm, á 1, sterile04054858030128
32134-104054858030135