Skip to content

Anchor Screw

by Institut Straumann AG 2 variants

Ref 048.386

Anchor Screw (048.386) is a Class IIb device made by Institut Straumann AG, registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 0763003170128QV), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763003170128QV Basic UDI-DI 07630031782083UDI-DIDate23 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Anchor Screw
Model / reference
048.386
Primary DI / UDI-DI
07630031782083
Basic UDI-DI
0763003170128QV
Unit of use DI
07630031787835
EMDN code
P01020101 Dental implants
Device class
Class IIb
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 DENTAL IMPLANTS.

Other devices from Institut Straumann AG

See all devices from Institut Straumann AG →

Properties

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