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Medtronic Reusable Instruments X0219021

by Medtronic Sofamor Danek, Inc.

Medtronic Reusable Instruments X0219021 is a Class I device made by Medtronic Sofamor Danek, Inc., listed in FDA GUDID since 8 Oct 2022 (UDI-DI 00763000274665), 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 Number00763000274665 UDI-DI Date8 Oct 2022ListedStatusListed 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  • Withdrawn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
Medtronic Reusable Instruments
Generic name
Bone tap, reusable
Model / reference
X0219021
Primary DI / UDI-DI
00763000274665
FDA product code
HWX
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

Similar devices in this category

Other devices filed under Bone tap, reusable.

Other devices from Medtronic Sofamor Danek, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)