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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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Unisex abdominal binder — 4 UDI-DI variants, MDR (Eto Garments ApS)

MD Atlas
Eto Garments ApS

Data from EUDAMED, last updated May 23, 2026

Unisex abdominal binder

571269000009A6

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: Eto Garments ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 571269000009A6
Device name: Unisex abdominal binder
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KR0NK1F13NBNXZTA5KMV5AB4

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

12005712690004323
12005712690004361
12005712690004316
12005712690004330