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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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AIR RING SUCTION — 12 UDI-DI variants, MDR (4TEK SRL)

MD Atlas
4TEK SRL

Data from EUDAMED, last updated May 31, 2026

AIR RING SUCTION

805084750AIR000009G

12 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: 805084750AIR000009G
Device name: —
Device model: AIR RING SUCTION
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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2NE7HZ9VAH46K67QJPBG1Y

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

A00108050847501569
A001/L08050847501576
A00208050847501583
A002-38008050847501590
A00308050847501606
A003T08050847501613
A00408050847501620
A004/L08050847501637
A00508050847501644
A00708050847501941
A007-38008050847501972
SS.PWD08050847504010