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Vista Plus

by Conlett Technology Inc

Ref TRANS2Model Vista Plus

Vista Plus (TRANS2) is a Class I device made by Conlett Technology Inc, registered in EUDAMED on 10 Nov 2024 (Basic UDI-DI 697359601VistaPlusF4), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697359601VistaPlusF4 Basic UDI-DI 06973596010200UDI-DIDate10 Nov 2024RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Vista Plus, TRANS2
Primary DI / UDI-DI
06973596010200
Basic UDI-DI
697359601VistaPlusF4
Direct marketing DI
06973596010200
EMDN code
W0202030202 Transilluminators
Device class
Class I
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000002101
Authorised representative
Lotus NL B.V. NL-AR-000000121

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Properties

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