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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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CAREPUR — 33 UDI-DI variants, MDR (SOFTLINE-Schaum GmbH & Co. KG)

MD Atlas
SOFTLINE-Schaum GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

CAREPUR

4056538POS001SJ

33 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: SOFTLINE-Schaum GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4056538POS001SJ
Device name: CAREPUR
Device model: Positionierungshilfen gefüllt (EPS/PP/PU)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: SOFTLINE-Schaum GmbH & Co. KG
SRN: DE-MF-000014549
Country: Germany
Email: info@softline-schaum.de
Phone: +493367840770

Variants by status

UDI-DI variants

33 UDI-DI variants

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Applied filters

basicUdiUlid01GPB7363MQZKAPVQF8M8YXT8R

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

P4377304056538004917
P4377204056538004900
P4377504056538004931
P4377104056538004894
P4381204056538005303
P4378004056538004986
P4377904056538004979
P4377804056538004962

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