Skip to content

Sectio Tray Standaard

by Medica Europe B.V.

Ref 109182AQ, 106091AV, 106091AR, 106091AU, 106091AP, 106091AS, 106091AQ

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8710685TF07001004S5 Basic UDI-DI Date14 Sep 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Custom Procedure Trays
Model / Reference
109182AQ, 106091AV, 106091AR, 106091AU, 106091AP, 106091AS, 106091AQ
Primary DI / UDI-DI
08710685117529, 08710685137886, 08710685116621, 08710685135325, 08710685101832, 08710685123384, 08710685114726
Basic UDI-DI
8710685TF07001004S5, 8710685TF07001003S3
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class III
Class IIb
Medical Purpose
No

Manufacturer details

EUDAMED SRN
NL-PR-000000117

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Other devices from Medica Europe B.V.

See all devices from Medica Europe B.V. →

Properties

  • Sterile