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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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Umbettungstuch / Umbettungslaken — 2 UDI-DI variants, MDR

MD Atlas
Reintex GmbH

Data from EUDAMED, last updated May 23, 2026

Umbettungstuch / Umbettungslaken

426243112RTUMBETT2G

2 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: Reintex GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426243112RTUMBETT2G
Device name: Umbettungstuch / Umbettungslaken
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Reintex GmbH
SRN: DE-MF-000041775
Country: Germany
Email: info@reintex.com
Phone: +496202 9276876

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9A6ZDCJ523CGGQE5F4R7G3S

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

RTUBT/S 04262431120214
RTUBT04262431120634