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Global Steptech 223000365

by Depuy (Ireland)

Global Steptech 223000365 is a Class I device made by Depuy (Ireland), listed in FDA GUDID since 14 Feb 2021 (UDI-DI 10603295525424), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295525424 UDI-DI Date14 Feb 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Global Steptech
Generic name
Surgical saw blade, oscillating, single-use
Model / Ref / Catalog
223000365
Primary DI / UDI-DI
10603295525424
FDA product code
KIJ
GMDN term
Surgical saw blade, oscillating, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical saw blade, oscillating, single-use

Other devices from Depuy (Ireland)

See all devices from Depuy (Ireland) →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)