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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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SMART STATION — 10 UDI-DI variants, MDR (4TEK SRL)

MD Atlas
4TEK SRL

Data from EUDAMED, last updated May 31, 2026

SMART STATION

805084750SMARTST0B3

10 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: 4TEK SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805084750SMARTST0B3
Device name: —
Device model: SMART STATION
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: 4TEK SRL
SRN: IT-MF-000014881
Country: Italy
Email: contact@4-tek.it
Phone: +39 02 91082211

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS23BV46ES637ND1A6NS9XQG

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

COROCK01E08050847502405
COROCK02E08050847502429
SM1E08050847504799
SM1EA08050847504812
SM2E08050847504775
SM2EA08050847504836
SM2N08050847504768
COSTONE1N08050847502351
COSTONE1E08050847502368
COSTONE2E08050847502382