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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 — 11 UDI-DI variants, MDR (Etac A/S)

MD Atlas
Etac A/S

Data from EUDAMED, last updated May 31, 2026

Ceiling Hoist

570799510TA

11 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: 570799510TA
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

11 UDI-DI variants

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Applied filters

basicUdiUlid01K21Y9CGV6K8QHG9SR59SVDXR

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 20005707995035516
Molift Air 20005707995032928
Molift Air 20005707995035509
Molift Air 20005707995032904
Molift Air 20005707995033888
Molift Air 35005707995032997
Molift Air 35005707995032966
Molift Air 35005707995033000
Molift Air 35005707995033017
Molift Air 35005707995032980
Molift Air 35005707995032973