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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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Quicksuite OR Table kits — 12 UDI-DI variants, MDR

MD Atlas
Medline International France SAS

Data from EUDAMED, last updated May 19, 2026

Quicksuite OR Table kits

0888277DC147NSKG

12 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: Medline International France SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0888277DC147NSKG
Device name: Quicksuite OR Table kits
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medline International France SAS
SRN: FR-MF-000000676
Country: France
Email: stanley.dorvilly@medline.com

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01KBR5AVANMDHH1XRHGQ0WR6C8

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

QUICKSUITE10888277432949
QUICKSUITE10888277423657
DYND4090E10888277424814
QSACOVER10888277604186
QSHPC10888277431157
DYNDE4090FTD20888277435305
SL80220E00888277447564
QSLCEL0110888277434219
DYKQSHPC1CEA40888277600509
DYND4090NA20888277436289
QSACEL0110888277434202
QSS0120888277430461