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Attune Solo Velys 2544-00-213

by Depuy (Ireland)

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295531807 UDI-DI Date10 Jun 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Attune Solo Velys
Generic Name
Joint prosthesis implantation kit, single-use
Model / Ref / Catalog
2544-00-213, 254400213
Primary DI / UDI-DI
10603295531807
FDA Product Code
JWH, MBH
GMDN Term
Joint prosthesis implantation kit, single-use
Device Class
Class II
Regulation Number
888.3560, 888.3565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Joint prosthesis implantation kit, single-use

Other devices from Depuy (Ireland)

See all devices from Depuy (Ireland) →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No