Skip to content

Appasamy

by Appasamy Associates Private Limited 796 variants

Part of a family of 60 devices: see the family page

Ref AA 7891

Appasamy (AA 7891) is a Class IIa device made by Appasamy Associates Private Limited, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 89043437MSI/CANNULASRR), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number89043437MSI/CANNULASRR Basic UDI-DI 08904343723010UDI-DIDate5 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Ocular Irrigation or Suction Cannulas, Reusable
Model / reference
AA 7891
Primary DI / UDI-DI
08904343723010
Basic UDI-DI
89043437MSI/CANNULASRR
EMDN code
L1713 Ocular irrigation or suction cannulas, reusable
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
IN-MF-000012093
Authorised representative
Amstermed B.V. NL-AR-000001971

Similar devices in this category

Other devices filed under OCULAR IRRIGATION OR SUCTION CANNULAS, REUSABLE.

Other devices from Appasamy Associates Private Limited

See all devices from Appasamy Associates Private Limited →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)