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Procedure pack

by GRI Medical & Electronic Technology Co., Ltd. 22 variants

Ref 86-01601-SModel URO-01

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69319181F084LH Basic UDI-DI 26931918100071UDI-DIDate12 Mar 2026RegisteredStatusActive

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  • Withdrawn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
Procedure pack
Model / Reference
URO-01, 86-01601-S
Primary DI / UDI-DI
26931918100071
Basic UDI-DI
69319181F084LH
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
The indications for use of Procedure packs will be determined by the physician based upon the specific type of procedure and products required to perform the procedure.

Manufacturer details

EUDAMED SRN
CN-PR-000013744

Related devices

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

Other devices from GRI Medical & Electronic Technology Co., Ltd.

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Properties

  • Sterile