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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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ESTASI — 34 UDI-DI variants, MDR (TECHNOGEL ITALIA SRL)

MD Atlas
TECHNOGEL ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

ESTASI

805127760ESTASIEP

34 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: TECHNOGEL ITALIA SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805127760ESTASIEP
Device name: ESTASI
Device model: Materasso antidecubito
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: TECHNOGEL ITALIA SRL
SRN: IT-MF-000034169
Country: Italy
Email: info@technogel.it
Phone: +390444463811

Variants by status

UDI-DI variants

34 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMTK3CJJ94X90RP8T9SX9BS

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

QE7085200EUCE08051277605629
QE7090190EUCE08051277605605
QE7090195EUCE08051277603878
QE7090200EUCE08051277605612
QE7090210EUCE08051277606831
QEE160190EUCE08051277605865
QEE160200EUCE08051277604714
QEE180195EUCE08051277605421
QEE200200EUCE08051277604790

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