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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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Patiententransporthilfe Rutschbrett — 11 UDI-DI variants, MDR

MD Atlas
Transatlantic HG Stolpe & Co. mbH

Data from EUDAMED, last updated May 23, 2026

Patiententransporthilfe Rutschbrett

4050856TRBD5

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: Transatlantic HG Stolpe & Co. mbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4050856TRBD5
Device name: Patiententransporthilfe Rutschbrett
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Transatlantic HG Stolpe & Co. mbH
SRN: DE-MF-000009432
Country: Germany
Email: info@transat.de
Phone: +49 0 6081 9430 50

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H93A778G2JQEQ74V4ZWMMTZY

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

meinHOLTZ Casual04050856041968
meinHOLTZ Casual04050856039446
MH-H0104050856039408
meinHOLTZ Nature04050856039477
MH-O0104050856044969
meinHOLTZ Timeless04050856039460
MH-T0104050856039453
MH-T0204050856041975
441106804050856016348
441110204050856016386
441108004050856016362