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Q Insertion Screw

by Synthes GmbH 10 variants

Part of a family of 10 devices: see the family page

Ref 04.228.516Model Q Insertion Screw

Q Insertion Screw (04.228.516) is a Class IIb device made by Synthes GmbH, registered in EUDAMED on 22 Aug 2025 (Basic UDI-DI 7611819a00801JS), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7611819a00801JS Basic UDI-DI 07612334115270UDI-DIDate22 Aug 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Q Insertion Screw
Model / reference
Q Insertion Screw, 04.228.516
Primary DI / UDI-DI
07612334115270
Basic UDI-DI
7611819a00801JS
EMDN code
P09120603 Cannulated screws
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CH-MF-000013345
Authorised representative
DePuy Ireland UC IE-AR-000009328

Similar devices in this category

Other devices filed under CANNULATED SCREWS.

Other devices from Synthes GmbH

  • Tomofix

    Class IIb

  • 03.111.100S

    Class IIb

  • 68.134.011

    Class II

  • Volt 68.134.111

    Class II

See all devices from Synthes GmbH →

Properties

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