Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

LIQUID RING SUCTION — 22 UDI-DI variants, MDR (4TEK SRL)

MD Atlas
4TEK SRL

Data from EUDAMED, last updated May 31, 2026

LIQUID RING SUCTION

805084750OEP00000EU

22 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805084750OEP00000EU
Device name: —
Device model: LIQUID RING SUCTION
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 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

22 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KS5684G23B38XNHBTZ612R8Y

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

OEP1003508050847501880
OEP1106008050847501705
OEP11060-38008050847501712
P00108050847501729
P001-38008050847501736
P001/P08050847501781
P001-380/P08050847501798
P001/S08050847501743
P001-380/S08050847501750
P001/SB08050847501767
P001-380/SB08050847501774
P001/T08050847501804
P001-380/T08050847501811
P001/TB08050847501828
P001-380/TB08050847501835
P00208050847501897
P002/S08050847501903
P002-60/S08050847502207
UCA108050847501842
UCA1-38008050847501859
UCA1-380/P08050847501873
UCA208050847501910