Skip to content

Esenta 423290

by Convatec, Purchasing Department

Ref 423290Model Sting Free Adh Rem Spray Sterile

Esenta 423290 is a Class I device made by Convatec, Purchasing Department, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 768455OST0029FK) and listed in FDA GUDID since 30 Sep 2022 (UDI-DI 00768455193042), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number768455OST0029FK Basic UDI-DI 00768455193042UDI-DIDate8 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00768455193042 UDI-DI Date30 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 768455OST0029FK registered 8 Oct 2026 Active
  • FDA GUDID UDI-DI 00768455193042 listed 30 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00768455193042
  2. Registered EUDAMED 768455OST0029FK

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  • Withdrawn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
Esenta
Generic name
Patient medical adhesive remover
Device name
Sting Free Adh Rem Spray Sterile
Model / reference
423290, Sting Free Adh Rem Spray Sterile
Primary DI / UDI-DI
00768455193042
Basic UDI-DI
768455OST0029FK
FDA product code
EXE
EMDN code
A108005 Devices for the removal of adhesives from the peristomal skin
GMDN term
Patient medical adhesive remover
Device class
Class I
Regulation number
876.5900
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 150.00000 Milliliter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Supplied sterileEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Supplied sterile UDI-DI 00768455193042: EUDAMED states No, FDA GUDID states Yes.

Related devices

Category: Patient medical adhesive remover

Similar devices in this category

Other devices filed under DEVICES FOR THE REMOVAL OF ADHESIVES FROM THE PERISTOMAL SKIN.

Other devices from Convatec, Purchasing Department

See all devices from Convatec, Purchasing Department →

Properties

  • Supplied sterile NoEUDAMEDYesGUDID
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)