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Coloplast 2310

by Coloplast A/S

Ref 2310

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number57089322976939K Basic UDI-DI Date11 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05701780079778 UDI-DI Date8 Apr 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

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  • Withdrawn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
Coloplast
Generic Name
Pressure bandage, non-latex, single-use
Device Name
Coloplast Rings accessory for skin protection
Model / Ref / Catalog
2310
Description
Coloplast Rings. Pre-cut 10 mm.
Primary DI / UDI-DI
05701780079778 EUDAMED
05701780123105 EUDAMED
00762123001073 GUDID
Basic UDI-DI
57089322976939K
Unit of Use DI
05708932966740, 05701780021203
FDA Product Code
NEC
EMDN Code
A108001 Rings / bezels / plates for peristomal skin
GMDN Term
Pressure bandage, non-latex, single-use
Device Class
Class I
Regulation Number
880.5090
EU market of registration
Germany
Ireland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Lumen/Inner Diameter — 10 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
05701780079778
05701780123105
GUDID
00762123001073

Related devices

Category: Pressure bandage, non-latex, single-use

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Sterile: No
  • 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
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No