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Furlow

by Coloplast A/S

Ref QB5555

Furlow (QB5555) is a Class I device made by Coloplast A/S, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 570893255573897TV), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number570893255573897TV Basic UDI-DI 03600040253878UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Furlow cylinder inserter
Model / reference
QB5555
Primary DI / UDI-DI
03600040253878
Basic UDI-DI
570893255573897TV
EMDN code
L06050199 Non-endoscopic urological dilation instruments, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
DK-MF-000025526

Similar devices in this category

Other devices filed under UROLOGY INSTRUMENTS, REUSABLE.

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)