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FlexTip Plus Epidural Set

by Arrow International LLC (Subsidiary of Teleflex Incorporated) 4 variants

Ref JC-05400-LL2

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000120K3 Basic UDI-DI 10801902197648UDI-DIDate2 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Anesthesia Procedure Packs - Catheters
Model / Reference
JC-05400-LL2
Primary DI / UDI-DI
10801902197648
Basic UDI-DI
08019020000000000000120K3
EMDN Code
N02010199 Peridural / epidural spinal catheters and kits - other
Device Class
Class IIb
Medical Purpose
The procedure packs contain CE-marked medical devices, which are packaged together and shipped to a customer upon request for physician/medical professional use. The devices can be used together or used individually. Epidural catheter permits access to the epidural space for the administration of epidural anaesthetic

Manufacturer details

EUDAMED SRN
US-PR-000023158

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Properties

  • Sterile