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Straumann® Falcon

by Institut Straumann AG

Ref FA1000

Straumann Falcon (FA1000) is a medical device (EU MDR Class IIa; EMDN category surgical navigation system) made by Institut Straumann AG, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 0763003170022QC), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763003170022QC Basic UDI-DI Date5 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Straumann® Falcon
Model / reference
FA1000
Primary DI / UDI-DI
07630031772398, 07630031787989
Basic UDI-DI
0763003170022QC, 0763003170127QT
EMDN code
Z12011401 Surgical navigation system
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000009933
Authorised representative
Etkon GmbH DE-AR-000009335

Similar devices in this category

Other devices filed under SURGICAL NAVIGATION SYSTEM.

Other devices from Institut Straumann AG

See all devices from Institut Straumann AG →

Properties

Other properties (14, all answered No)