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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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Lagerungs- und Positionierungshilfe… — 6 UDI-DI variants, MDR

MD Atlas
Enste PhysioForm Reha GmbH

Data from EUDAMED, last updated May 23, 2026

Lagerungs- und Positionierungshilfe Malta Standard

426074058255

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: Enste PhysioForm Reha GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074058255
Device name: Lagerungs- und Positionierungshilfe Malta Standard
Device model: Malta Standard PhysioTex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: Enste PhysioForm Reha GmbH
SRN: DE-MF-000014095
Country: Germany
Email: info@enste-reha.de
Phone: 0672142464

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G7PS3BT99N7HT2J2X3RCEGG5

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

65941BW04260740580422
6594104260740580408
65941ST04260740580415
65951BW04260740580385
6595104260740580361
65951ST04260740580378