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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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Assistive manual aid for persons with… — 8 UDI-DI variants, MDR

MD Atlas
Liko Aktiebolag

Data from EUDAMED, last updated May 31, 2026

Assistive manual aid for persons with a disability

0887761GMN000039UF

8 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: Liko Aktiebolag

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0887761GMN000039UF
Device name: Assistive manual aid for persons with a disability
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Liko Aktiebolag
SRN: SE-MF-000001404
Country: Sweden
Email: quality_lulea@baxter.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KCQ2X4W18HZMT6HJ79RV0T7Q

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

HandyBelt00887761979703
HandyBelt00887761979673
HandyBelt00887761979680
HandyBelt00887761979697
Liko00887761968585
Liko00887761968592
Liko00887761968608
Liko00887761968578