Skip to content

Foxseal FG08814441

by Medtrade Products, Ltd.

Ref FG08814441

Foxseal FG08814441 is a device classified as Class IIb in the EU and Class I in the US made by Medtrade Products, Ltd., registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI B-15060206630632) and listed in FDA GUDID since 30 Jun 2020 (UDI-DI 15060206630632), active as of 25 Oct 2026.

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

CE MDD

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-15060206630632 Basic UDI-DI 15060206630632UDI-DIDate16 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number15060206630632 UDI-DI Date30 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-15060206630632 registered 16 Sep 2026 Active
  • FDA GUDID UDI-DI 15060206630632 listed 30 Jun 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 15060206630632
  2. Registered EUDAMED B-15060206630632

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Foxseal
Generic name
Pneumothorax dressing
Device name
Pneumothorax Dressing
Model / Ref / Catalog
FG08814441
Primary DI / UDI-DI
15060206630632
Basic UDI-DI
B-15060206630632
FDA product code
NAD
EMDN code
M04040501 Hydrogel dressings, non-combined
GMDN term
Pneumothorax dressing
Device class
Class IIb EUDAMED
Class I GUDID
Regulation number
878.4020
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Width — 5.24 Inch
Length — 5.12 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class I

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Pneumothorax dressing

Similar devices in this category

Other devices filed under HYDROGEL DRESSINGS, NON-COMBINED.

Other devices from Medtrade Products, Ltd.

See all devices from Medtrade Products, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
Other properties (19, all answered No)