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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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Gynstolar — 66 UDI-DI variants, MDR (Sjöbloms Sjukvårdsutrustning AB)

MD Atlas
Sjöbloms Sjukvårdsutrustning AB

Data from EUDAMED, last updated May 31, 2026

Gynstolar

73315086AX

66 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: 73315086AX
Device name: Gynstolar
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

66 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KFB8XF3HNCPF2V2N2PVEWEVG

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

No registered UDI-DI variants for this device family.