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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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Facial compression garment — 43 UDI-DI variants, MDR

MD Atlas
Eto Garments ApS

Data from EUDAMED, last updated May 23, 2026

Facial compression garment

5712690000019N

43 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: Eto Garments ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5712690000019N
Device name: Facial compression garment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eto Garments ApS
SRN: DK-MF-000002251
Country: Denmark
Email: ag@eto-garments.com
Phone: 004564461330

Variants by status

UDI-DI variants

43 UDI-DI variants

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Applied filters

basicUdiUlid01KQF30ENC0QMSTFXMC6GH6238

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

20405712690006358
20005712690006167
20605712690006372
20105712690006280
20905712690006433
20605712690006402
20205712690006303
20005712690006204
20105712690006242
20605712690016289
20105712690006259
20005712690006198
20005712690006235
20905712690016395
21005712690006525
20605712690006389
20905712690006501
20005712690016296

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