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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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Dia-Stop — 2 UDI-DI variants, MDR (LiNA Medical AG)

MD Atlas
LiNA Medical AG

Data from EUDAMED, last updated May 23, 2026

Dia-Stop

57082653002-1SQV

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: LiNA Medical AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57082653002-1SQV
Device name: Dia-Stop
Device model: 8055-01n, 8065-Cn
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: LiNA Medical AG
SRN: CH-MF-000046832
Country: Switzerland
Email: plu@lina-medical.com
Phone: +48 789 105 422

Authorised representative

Name: LiNA Medical Polska Sp. z o.o.
SRN: PL-AR-000039364
Country: Poland
Phone: +48 61 222 21 21

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KJ5A07Z0RT6T7MWJ3W136KJR

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

Dia-Stop05708265017126
Dia-Stop Cushion05708265017171