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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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Wall Brackets — 7 UDI-DI variants, MDR (Serres Oy)

MD Atlas
Serres Oy

Data from EUDAMED, last updated May 23, 2026

Wall Brackets

6418685SBS132R

7 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: Serres Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6418685SBS132R
Device name: Wall Brackets
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: Serres Oy
SRN: FI-MF-000004504
Country: Finland
Email: quality@serres.com
Phone: +358 20 746 4400

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01FTX2ABW99KM61SMCC759WNBG

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

57081706418685049506
5781706418685000095
5782006418685000064
57820-906418685023926
57082006418685062727
57081406418685062710
5781406418685043313