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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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FIXED EXPANDER — 177 UDI-DI variants, MDR (LEONE S.P.A.)

MD Atlas
LEONE S.P.A.

Data from EUDAMED, last updated May 31, 2026

FIXED EXPANDER

080337070TDIIA001M03-8J

177 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: LEONE S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 080337070TDIIA001M03-8J
Device name: —
Device model: FIXED EXPANDER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: LEONE S.P.A.
SRN: IT-MF-000005986
Country: Italy
Email: info@leone.it

Variants by status

UDI-DI variants

177 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNVVESFZYVDFXGV17A8ZD3KP

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

A0640-10D08033707103226
A1621P90808033707093893

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