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Leukomed® 72390-03

by Bsn Medical SAS

Ref 72390-03

Leukomed® 72390-03 is a Class I device made by Bsn Medical SAS, registered in EUDAMED on 29 Jul 2026 (Basic UDI-DI 4042809400416508N) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 04042809269925), active as of 8 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4042809400416508N Basic UDI-DI 04042809269925UDI-DIDate29 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04042809269925 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4042809400416508N registered 29 Jul 2026 Active
  • FDA GUDID UDI-DI 04042809269925 listed 8 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04042809269925
  2. Registered EUDAMED 4042809400416508N

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Leukomed®
Generic name
Skin-cover adhesive strip, non-antimicrobial
Device name
Leukomed® I.V. film
Model / Ref / Catalog
72390-03
Primary DI / UDI-DI
04042809269925
Basic UDI-DI
4042809400416508N
Unit of use DI
04042809667608
FDA product code
NAD
EMDN code
M050199 Surgical plasters - other
GMDN term
Skin-cover adhesive strip, non-antimicrobial
Device class
Class I
Regulation number
878.4020
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 11.5 Centimeter
Width — 8.5 Centimeter

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Other devices filed under SURGICAL PLASTERS.

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Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)