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Dinamic T Humerus

by Citieffe 5 variants

Part of a family of 29 devices: see the family page

Ref DT070002Model GUIDE WIRES

Dinamic T Humerus (DT070002) is a device classified as Class I in the EU and Class II in the US made by Citieffe, registered in EUDAMED on 11 Jun 2026 (Basic UDI-DI 803290962117BX), cleared under FDA 510(k) K113387 on 15 Mar 2012 and listed in FDA GUDID since 4 Jul 2022 (UDI-DI 08052990971510), active as of 25 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K113387

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number803290962117BX Basic UDI-DI 08052990971510UDI-DIDate11 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08052990971510 UDI-DI Date4 Jul 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK113387 Date15 Mar 2012DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 803290962117BX registered 11 Jun 2026 Active
  • FDA 510(k) K113387 decided 15 Mar 2012 Active
  • FDA GUDID UDI-DI 08052990971510 listed 4 Jul 2022 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K113387
  2. Listed FDA GUDID 08052990971510
  3. Registered EUDAMED 803290962117BX

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Surgical Instruments (Ir) EUDAMED
Dinamic T Humerus GUDID
Generic name
Orthopaedic guidewire, reusable
Model / Ref / Catalog
GUIDE WIRES, DT070002, Graduated guide wire with olive ø2.5mmx450mm
Primary DI / UDI-DI
08052990971510
Basic UDI-DI
803290962117BX
Direct marketing DI
08052990971510
510(k) Number
FDA product code
HSB
EMDN code
L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
GMDN term
Orthopaedic guidewire, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3020
EU registration type
Standard device
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
GUIDE WIRES
DT070002
GUDID
Graduated guide wire with olive ø2.5mmx450mm
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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 guidewire, reusable

Cleared under the same submission (K113387)

and 8 more cleared under K113387

Similar devices in this category

Other devices filed under INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from Citieffe

See all devices from Citieffe →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)