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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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ECO — 36 UDI-DI variants, MDR (4TEK SRL)

MD Atlas
4TEK SRL

Data from EUDAMED, last updated May 31, 2026

ECO

805084750ECO000007F

36 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: 805084750ECO000007F
Device name: —
Device model: ECO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 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

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR3FR85X92707J6Z7QFC9TBS

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

SS.APL1.ES08050847504348
SS.APL208050847504317
SS.APL2.E08050847504324
SS.APL2.E_6008050847504614
SS.APL2.ES08050847504362
COTOP2N2208050847500623
COTO2236E08050847500630
COTO2238E08050847500654
COTO3S22008050847500661
COTOP322008050847500678
COTOP338E08050847500692

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