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Robot Uro Buik Tray

by Medica Europe B.V. 2 variants

Ref 110542AS, 110542AI, 110542AO, 110542AR, 110542AQ, 110542AT

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 Number8710685TF07001002RZ Basic UDI-DI Date14 Mar 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  • Withdrawn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
110542AS, 110542AI, 110542AO, 110542AR, 110542AQ, 110542AT
Primary DI / UDI-DI
08710685132751, 08710685078646, 08710685121212, 08710685130023, 08710685126835, 08710685147380
Basic UDI-DI
8710685TF07001002RZ, 8710685TF07001004S5
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIa
Class III
Medical Purpose
No

Manufacturer details

EUDAMED SRN
NL-PR-000000117

Related devices

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

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Properties

  • Sterile