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Again Pro Plus

by Deka M.E.L.A. SRL 3 variants

Ref M126U1, M126E1, M126H1, M126Q1, M126Z1, M126G1, M126F1, M126V1

Again Pro Plus (M126U1) is a Class IIb device made by Deka M.E.L.A. SRL, registered in EUDAMED on 17 Feb 2026 (Basic UDI-DI B-08034108512389), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08034108512389 Basic UDI-DI Date17 Feb 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Trade name
Again Pro Plus
Again
Again Pro
Model / reference
M126U1, M126E1, M126H1, M126Q1, M126Z1, M126G1, M126F1, M126V1
Primary DI / UDI-DI
08034108512389, 08034108510958, 08034108510989, 08034108511948, 08034108512457, 08034108510972, 08034108510965, 08034108512440
Basic UDI-DI
B-08034108512389, B-08034108510958, B-08034108510989, B-08034108511948, B-08034108512457, B-08034108510972, B-08034108510965, B-08034108512440
EMDN code
Z12011012, Z12011019, Z12011017
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007389

From the manufacturer

Manufacturer's product page: Again PRO PLUS

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Properties

Other properties (12, all answered No)