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MISHA® Torque Limiting Driver 1-4039

by Moximed, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856047005917 UDI-DI Date5 May 2023ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MISHA® Torque Limiting Driver
Generic Name
Orthopaedic surgical procedure kit, non-medicated, single-use
Model / Reference
1-4039
Primary DI / UDI-DI
00856047005917
De Novo Number
FDA Product Code
QVV
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, single-use
Device Class
Class II
Regulation Number
888.3610
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic surgical procedure kit, non-medicated, single-use

Cleared under the same submission (DEN220033)

Other devices from Moximed, Inc.

See all devices from Moximed, Inc. →

Properties

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

Other properties (9)

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