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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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Ceiling Hoist — 14 UDI-DI variants, MDR (Etac A/S)

MD Atlas
Etac A/S

Data from EUDAMED, last updated May 31, 2026

Ceiling Hoist

57079957ES

14 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: Etac A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57079957ES
Device name: —
Device model: Ceiling Hoist
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Etac A/S
SRN: DK-MF-000017724
Country: Denmark
Email: info@etac.dk
Phone: +45 79685833

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01K21Y9B6Z0EHNEZX8CP00WKRF

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

Molift Air 20505707995033031
Molift Air 20505707995032935
Molift Air 20505707995032829
Molift Air 20505707995032836
Molift Air 20505707995032942
Molift Air 20505707995033055
Molift Air 20505707995032812
Molift Air 20505707995033499
Molift Air 20505707995033505
Molift Air 30005707995032959
Molift Air 30005707995033512
Molift Air 30005707995033048
Molift Air 30005707995033062
Molift Air 30005707995032867