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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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Suction tubing — 11 UDI-DI variants, MDR

MD Atlas
Medline International France SAS

Data from EUDAMED, last updated May 19, 2026

Suction tubing

0888277DC163ASTK9

11 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: 0888277DC163ASTK9
Device name: Suction tubing
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KEFPX19F4B36FEX9721YBS2P

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

TUB101010888277425415
TUB1010H10888277425439
TUB10610888277425408
RSC24F10888277420908
TUB106H10888277425422
ORS78SF00888277437015
RSC15F10888277420892
TUBH10888277432956
ORS71000888277437039
ORS78S00888277437008
NBT7800888277437022