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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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LUVAR — 13 UDI-DI variants, MDR (Heyer Medical AG)

MD Atlas
Heyer Medical AG

Data from EUDAMED, last updated May 23, 2026

LUVAR

4251743800006UT

13 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: Heyer Medical AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4251743800006UT
Device name: LUVAR
Device model: Many
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Heyer Medical AG
SRN: DE-MF-000014330
Country: Germany
Email: yxiang@heyermedical.de
Phone: +49 2603 791 340

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01GTV3MBQEGMPM7W7T0PVSK89R

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

12110004251743800082
12200104251743800211
12200204251743800228
12200304251743800235
12200404251743800242
12200504251743800259
12200604251743800266
12200704251743800273
12200804251743800204
12200904251743800280
12201004251743800297
12201104251743800303
LUVAR STA04251743800068