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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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FloorLine-i EU — 3 UDI-DI variants, MDR (Human Care HC AB)

MD Atlas
Human Care HC AB

Data from EUDAMED, last updated May 30, 2026

FloorLine-i EU

7331599BA009030090303ZL

3 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: Human Care HC AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7331599BA009030090303ZL
Device name: FloorLine-i EU
Device model: 90300
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 20, 2021

Manufacturer & authorised representative

Manufacturer

Name: Human Care HC AB
SRN: SE-MF-000002090
Country: Sweden
Email: info.se@humancaregroup.com
Phone: +46 8 510 132 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FQBWSENKYK5DT4KSVP9W64CN

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

9030107331599440698
9030007331599440230
9030307331599440704