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Coflex NL TAN, 3" X 5 Yds

by Andover Healthcare Inc.

Ref 5300TN-024Model CoFlex NL

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 Number0724004CoFlexNLQG Basic UDI-DI 00724004531079UDI-DIDate25 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724004531079 UDI-DI Date5 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  • Withdrawn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
Coflex NL
Generic Name
Pressure bandage, non-latex, single-use
Device Name
Coflex
Model / Ref / Catalog
CoFlex NL, 5300TN-024, TAN, 3" X 5 Yds
Primary DI / UDI-DI
00724004531079 EUDAMED
10724004531076 GUDID
Basic UDI-DI
0724004CoFlexNLQG
FDA Product Code
FQM
EMDN Code
M030402020101 Elastic support bandages, cohesive, extensible in one direction, high extensibility
GMDN Term
Pressure bandage, non-latex, single-use
Device Class
Class I
Regulation Number
880.5075
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
CoFlex NL
5300TN-024
GUDID
TAN, 3" X 5 Yds
Primary DI / UDI-DIEUDAMED
00724004531079
GUDID
10724004531076

Other devices from Andover Healthcare Inc.

See all devices from Andover Healthcare Inc. →

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