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Do-All

by Doall 26 variants

Ref RF NEEDLE

Do-All (RF NEEDLE) is a Class IIa device made by Doall, registered in EUDAMED on 29 Aug 2024 (Basic UDI-DI B-08800145302913), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800145302913 Basic UDI-DI Date29 Aug 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Rfn-09F32G
Rfn-09S31G
Rfn-05P33G
Rfn-05P31G
Model / reference
RF NEEDLE
Primary DI / UDI-DI
08800145302913, 08800145302937, 08800145302982, 08800145302968
Basic UDI-DI
B-08800145302913, B-08800145302937, B-08800145302982, B-08800145302968
EMDN code
K02030101 Radiofrequency surgery electrodes, single-use
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000037741
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under RADIOFREQUENCY SURGERY ELECTRODES, SINGLE-USE.

Other devices from Doall

See all devices from Doall →

Properties

  • Supplied sterile
Other properties (11, all answered No)