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Glide

by Aurolab

Ref NilModel C100-DI100,C200-DI100,C300-DI150,AC28-DI100,AC22-DI260Y,C300-DI100,AC28P-PL2, AC22P - PL2,C290

Glide (Nil) is a Class IIa device made by Aurolab, registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI B-803878CDI001XMST), 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-803878CDI001XMST Basic UDI-DI D-803878CDI001XMSTUDI-DIDate13 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Injectors and catridges for injecting of Foldable lenses
Model / reference
C100-DI100, C200-DI100, C300-DI150, AC28-DI100, AC22-DI260Y, C300-DI100, AC28P-PL2, AC22P - PL2, C290, Nil
Primary DI / UDI-DI
D-803878CDI001XMST
Basic UDI-DI
B-803878CDI001XMST
EMDN code
Q021199 Ophthalmic surgery instruments, single-use - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000007255
Authorised representative
mdi Europa GmbH DE-AR-000006218

Similar devices in this category

Other devices filed under OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Aurolab

See all devices from Aurolab →

Properties

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