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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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Patient transfer sheet, non sterile — 2 UDI-DI variants, MDR

MD Atlas
Mercator Medical Spółka Akcyjna

Data from EUDAMED, last updated May 31, 2026

Patient transfer sheet, non sterile

5906615W76NSNWXP

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: Mercator Medical Spółka Akcyjna

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5906615W76NSNWXP
Device name: Patient transfer sheet, non sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mercator Medical Spółka Akcyjna
SRN: PL-MF-000018942
Country: Poland
Email: regulatory@pl.mercatormedical.eu
Phone: +48 667 095 924

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KKGR9WTHV7QR5Z2ZK2RJJ3P2

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

SAFELINE PAD Patient transfer sheet, non-sterile05906615041337
SAFELINE PAD Patient transfer sheet, with absorbent pad, non-sterile05906615041313