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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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Toilettensitzerhöhung RFM 5 cm mit… — 6 UDI-DI variants, MDR

MD Atlas
Rehaforum Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Toilettensitzerhöhung RFM 5 cm mit Deckel

4041314toilettensitz6S

6 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: Rehaforum Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4041314toilettensitz6S
Device name: Toilettensitzerhöhung RFM 5 cm mit Deckel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Rehaforum Medical GmbH
SRN: DE-MF-000018288
Country: Germany
Email: info@rehaforum.com
Phone: +49 4121 473312

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K1831FT9129KEXTYBMJC5TR3

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

0608719504041314024296
0608720304041314024302
0252271904041314026221
0250560304041314026214
0248435004041314026207
0248187704041314026191