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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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Midline Kit — 9 UDI-DI variants, MDR (Delta Med SPA)

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 31, 2026

Midline Kit

8032248650009G

9 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: Delta Med SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8032248650009G
Device name: —
Device model: Midline Kit
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: Delta Med SPA
SRN: IT-MF-000027962
Country: Italy
Email: info@numantec.eu

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K107MYQE6FAWRZRRF40D1CEB

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

DELTA MIDLINE 3Frx1Lx25cm-IM05NC08032248650367
DELTA MIDLINE 3Frx1Lx25cm-IM07NC08032248650374
DELTA MIDLINE 3Frx1Lx25cm-IM07NS08032248650015
DELTA MIDLINE 4Frx1Lx25cm-IM05NC08032248650428
DELTA MIDLINE 4Frx1Lx25cm-IM07NC08032248650435
DELTA MIDLINE 4Frx1Lx25cm-IM07NS08032248650077
DELTA MIDLINE 4Frx1Lx25cm-IM10NC08032248650442
DELTA MIDLINE 5Frx1Lx25cm-IM07NC08032248650497
DELTA MIDLINE 5Frx1Lx25cm-IM07NS08032248650138