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Aguja De Redón / Redon Needle

by Iberhospitex, S.A. 7 variants

Ref 0030007

Aguja De Redón / Redon Needle (0030007) is a Class IIa device made by Iberhospitex, S.A., registered in EUDAMED on 21 Sep 2026 (Basic UDI-DI 8428097AGUJA22), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8428097AGUJA22 Basic UDI-DI 08428097028608UDI-DIDate21 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Aguja De Redón / Redon Needle
Model / reference
0030007
Primary DI / UDI-DI
08428097028608
Basic UDI-DI
8428097AGUJA22
EMDN code
A019009 Drainage needles
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000160

Similar devices in this category

Other devices filed under NEEDLES FOR OTHER PROCEDURES.

Other devices from Iberhospitex, S.A.

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Properties

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