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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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Undersökningsbrits 3-delad elektrisk — 3 UDI-DI variants, MDR

MD Atlas
Sjöbloms Sjukvårdsutrustning AB

Data from EUDAMED, last updated May 31, 2026

Undersökningsbrits 3-delad elektrisk

73315084AT

3 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: Sjöbloms Sjukvårdsutrustning AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73315084AT
Device name: Undersökningsbrits 3-delad elektrisk
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sjöbloms Sjukvårdsutrustning AB
SRN: SE-MF-000005205
Country: Sweden
Email: urban@sjobloms.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KFB54SDE0ZPYC1FFMN2M7857

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

Examination table electric 3-sectioned07331508001613
Examination table electric 3-sectioned07331508006779
Patient trolley 3-sectioned electric07331508006816