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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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Safety Mattress — 6 UDI-DI variants, MDR (ZiboCare A/S)

MD Atlas
ZiboCare A/S

Data from EUDAMED, last updated May 23, 2026

Safety Mattress

5715841043306MFULT

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: ZiboCare A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5715841043306MFULT
Device name: —
Device model: Safety Mattress
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: ZiboCare A/S
SRN: DK-MF-000045317
Country: Denmark
Email: post@zibocare.dk
Phone: +45 76 900 407

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JXFH2E0M17DAMR85HZAAAKQD

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

MSKPR400705715841502488
MSKPR400805715841502495
MSKPR4008FP05715841502884
MSKPR400505715841502501
882006SIK05715841502518
MSKPR400605715841502525