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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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Gebärsysteme — 11 UDI-DI variants, MDR (Febromed GmbH & Co. KG)

MD Atlas
Febromed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Gebärsysteme

426074055TRACAX

11 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: Febromed GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074055TRACAX
Device name: Gebärsysteme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 9, 2023

Manufacturer & authorised representative

Manufacturer

Name: Febromed GmbH & Co. KG
SRN: DE-MF-000009287
Country: Germany
Email: info@febromed.de
Phone: +49 2522 9201900

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H7CKP4MTWEE4YBGE5M8SXB8F

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

DGH - ALU04260740550111
DGH04260740550104
PBall-5504260740550197
PBall-6504260740550203
CTRAC - 400004260740550142
DETTO-500004260740550128
MTRAC-600004260740550135
PTRAC-200004260740550159
VARIOD-795004260740550166
VARIOS-700004260740550180
VARIOW-700004260740550173