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Hv Screw System DHVS3038

by Wright Medical Technology, Inc.

Part of a family of 16 devices: see the family page

Ref DHVS3038Model 08897970033XT

Hv Screw System DHVS3038 is a device classified as Class IIb in the EU and Class II in the US made by Wright Medical Technology, Inc., registered in EUDAMED on 23 Jul 2026 (Basic UDI-DI 08897970033XT) and listed in FDA GUDID since 6 Dec 2017 (UDI-DI 00840420193544), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08897970033XT Basic UDI-DI 00840420193544UDI-DIDate23 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00840420193544 UDI-DI Date6 Dec 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08897970033XT registered 23 Jul 2026 Active
  • FDA GUDID UDI-DI 00840420193544 listed 6 Dec 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00840420193544
  2. Registered EUDAMED 08897970033XT

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Hv Screw System
Generic name
Orthopaedic bone screw, non-bioabsorbable, sterile
Device name
HV Screws Implants-Headless Cannulated Screw-Titanium Alloy-Anodized-Class IIb-Sterile
Model / Ref / Catalog
DHVS3038, 08897970033XT
Primary DI / UDI-DI
00840420193544
Basic UDI-DI
08897970033XT
FDA product code
HWC
EMDN code
P09120603 Cannulated screws
GMDN term
Orthopaedic bone screw, non-bioabsorbable, sterile
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3040
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Outer Diameter — 3 Millimeter
Length — 38 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Similar devices in this category

Other devices filed under CANNULATED SCREWS.

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Sutures
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)