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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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LiNA MaxFlow — 4 UDI-DI variants, MDR (LiNA Medical AG)

MD Atlas
LiNA Medical AG

Data from EUDAMED, last updated May 23, 2026

LiNA MaxFlow

57082651010-1YT

4 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: LiNA Medical AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57082651010-1YT
Device name: LiNA MaxFlow
Device model: SIV-100, SIV-105, SIP-010, SIP-005-370
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 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

4 UDI-DI variants

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Applied filters

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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

LiNA MaxFlow05708265016167
LiNA MaxFlow05708265016143
LiNA MaxFlow05708265016181
LiNA MaxFlow05708265016129