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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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Mediloops® Vessel Loop — 10 UDI-DI variants, MDR (Neuromedex GmbH)

MD Atlas
Neuromedex GmbH

Data from EUDAMED, last updated May 31, 2026

Mediloops® Vessel Loop

426002751100-015-1L6

10 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: Neuromedex GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426002751100-015-1L6
Device name: Mediloops® Vessel Loop
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Neuromedex GmbH
SRN: DE-MF-000005867
Country: Germany
Email: contact@neuromedex.com
Phone: +49 40 696 564 0

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KSSPN6PZZSX49H80Q0F7PN02

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

Mediloops® Vessel Loop04260027510449
Mediloops® Vessel Loop04260027510470
Mediloops® Vessel Loop04260027510487
Mediloops® Vessel Loop04260027510418
Mediloops® Vessel Loop04260027510463
Mediloops® Vessel Loop04260027510395
Mediloops® Vessel Loop04260027510401
Mediloops® Vessel Loop04260027510456
Mediloops® Vessel Loop04260027510432
Mediloops® Vessel Loop04260027510388