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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 — 8 UDI-DI variants, MDR (Etac A/S)

MD Atlas
Etac A/S

Data from EUDAMED, last updated May 31, 2026

Sling

570799527TT

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: Etac A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 570799527TT
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01JW69RNMY1ZWJZ5507BCTSW9H

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 RgoSling Repositioning Sheet05707995040190
Molift RgoSling Repositioning Sheet05707995040213
Molift RgoSling Repositioning Sheet05707995034953
Molift RgoSling Repositioning Sheet05707995000958
Molift RgoSling Repositioning Sheet05707995000972
Molift RgoSling Repositioning Sheet05707995040237
Molift RgoSling Repositioning Sheet05707995000941
Molift UnoSling Repositioning Sheet05707995036148