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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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Occluders — 6 UDI-DI variants, MDR (Luneau Technology Operations)

MD Atlas
Luneau Technology Operations

Data from EUDAMED, last updated May 19, 2026

Occluders

13664188000275M5

6 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: Luneau Technology Operations

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 13664188000275M5
Device name: Occluders
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Luneau Technology Operations
SRN: FR-MF-000009091
Country: France
Email: contact@visionix.com
Phone: +33 2 32 98 91 32

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KR20KTQK06A2J4Q6CERD5A6E

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

8630-1139-0503664188000695
8630-1510-2803664188000282
719004003664188000299
8630-1141-5403664188000701
8630-1650-1003664188000275
719003903664188000688