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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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LMA Supreme — 7 UDI-DI variants, MDR (Teleflex Medical)

MD Atlas
Teleflex Medical

Data from EUDAMED, last updated May 31, 2026

LMA Supreme

08019020000000000000213KB

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Teleflex Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08019020000000000000213KB
Device name: LMA Supreme
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Teleflex Medical
SRN: IE-MF-000015868
Country: Ireland
Email: orders.intl@teleflex.com
Phone: 353 (0) 9 06 46 08 00

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KSF4EYD6ZWEK8YVZHDXBZVN2

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

LMA® Supreme™ Size 115060112319881
LMA® Supreme™ Size 1.515060112319898
LMA® Supreme™ Size 215060112319904
LMA® Supreme™ Size 2.515060112319911
LMA® Supreme™ Size 315060112319928
LMA® Supreme™ Size 415060112319935
LMA® Supreme™ Size 515060112319942