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Administration Device

by Uroplasty, LLC

Ref ADModel Administration Device

Administration Device is a Class I device made by Uroplasty, LLC, registered in EUDAMED on 29 May 2026 (Basic UDI-DI 87175912404W6), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number87175912404W6 Basic UDI-DI 08717591240372UDI-DIDate29 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Administration Device, AD
Primary DI / UDI-DI
08717591240372
Basic UDI-DI
87175912404W6
EMDN code
U99 Devices for urogenital system - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000041660
Authorised representative
Medical Measurement Systems B.V. NL-AR-000010438

Similar devices in this category

Other devices filed under DEVICES FOR UROGENITAL SYSTEM - OTHER.

Other devices from Uroplasty, LLC

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Properties

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