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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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Seating — 17 UDI-DI variants, MDR (R82 A/S)

MD Atlas
R82 A/S

Data from EUDAMED, last updated May 23, 2026

Seating

570729218093957

17 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: R82 A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 570729218093957
Device name: —
Device model: Seating
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: R82 A/S
SRN: DK-MF-000000772
Country: Denmark
Email: R82@etac.com

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01KC46Q6A47W03GW8G0MRMMCXB

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

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x:panda05707292795236
x:panda05707292795137
x:panda05707292787163
x:panda shape05707292975737
x:panda shape05707292987174
x:panda shape05707292986955
x:panda shape05707292981684
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