Lumina Film dressing 5x7, 2

by Lumina Adhesives AB 2 variants

Ref 1000411

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number7350115661002V4 Basic UDI-DI 07350115662116UDI-DI	Date23 Nov 2022Registered	StatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name: Film dressing
Model / Reference: 1000411

Primary DI / UDI-DI: 07350115662116
Basic UDI-DI: 7350115661002V4
EMDN Code: M04040601 Polyurethane dressings, non-combined

Device Class: Class I
EU market of registration: Sweden

Manufacturer details

EUDAMED SRN: SE-MF-000000737

Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No