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PowerGlide Pro

by Bard Access Systems, Inc. 15 variants

Ref 6F120080

PowerGlide Pro (6F120080) is a Class IIa device made by Bard Access Systems, Inc., registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI B-0080174113861LCK), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-0080174113861LCK Basic UDI-DI D-0080174113861LCKUDI-DIDate23 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
BD PowerGlide Pro™ Midline Catheter, 18 G x 100 mm
Model / reference
6F120080
Primary DI / UDI-DI
D-0080174113861LCK
Basic UDI-DI
B-0080174113861LCK
EMDN code
V0599 Clinical procedures kits not included in other classes - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000017720
Authorised representative
Becton Dickinson Ireland Limited IE-AR-000007610

Similar devices in this category

Other devices filed under CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Bard Access Systems, Inc.

See all devices from Bard Access Systems, Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)