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Mighty Wire™ Initial Release

by Merit Medical Systems, Inc. 16 variants

Mighty Wire™ Initial Release (MW353004S) is a Class II device made by Merit Medical Systems, Inc., listed in FDA GUDID since 27 Sep 2024 (UDI-DI 00884450564035), 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 Number00884450564035 UDI-DI Date27 Sep 2024ListedStatusListed 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  • Withdrawn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
Mighty Wire™
Generic name
Cardiac/peripheral vascular guidewire, single-use
Model / Ref / Catalog
Initial Release, MW353004S
Primary DI / UDI-DI
00884450564035
FDA product code
DQX
GMDN term
Cardiac/peripheral vascular guidewire, single-use
Device class
Class II
Regulation number
870.1330
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiac/peripheral vascular guidewire, single-use

Similar devices in this category

Other devices filed under Cardiac/peripheral vascular guidewire, single-use.

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

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