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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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Inco slide — 4 UDI-DI variants, MDR (Swereco AB)

MD Atlas
Swereco AB

Data from EUDAMED, last updated May 31, 2026

Inco slide

73314270004M3

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: Swereco AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73314270004M3
Device name: —
Device model: Inco slide
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Swereco AB
SRN: SE-MF-000033314
Country: Sweden
Email: evelina.styhre@swereco.com
Phone: +46709578338

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNW60KHAJDHHQ2R3ZVNZWAV

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

Absorba inkoglid Hera07331427090941
Absorba inkoglid Zeus07331427090743
Absorba inkoglid Zeus, Textilia, HF-chip07331427000094
Absorba inkoglid Zeus, Textilia, UHF-chip07331427000100