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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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Sling — 4 UDI-DI variants, MDR (Etac A/S)

MD Atlas
Etac A/S

Data from EUDAMED, last updated May 31, 2026

Sling

570799517TQ

4 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: 570799517TQ
Device name: —
Device model: Sling
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01JVPXSQB0YA6VSA7F5M8JNG1X

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 EvoSling FlexiStrap05707995038340
Molift EvoSling FlexiStrap05707995001962
Molift UnoSling LimbLift05707995036131
Molift UnoSling LimbLift05707995036124