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Wound CareKit MDXWC02

by Mirodx, LLC 3 variants

Wound CareKit MDXWC02 (MDXWC021) is a Class II device made by Mirodx, LLC, listed in FDA GUDID since 23 Feb 2023 (UDI-DI 00860009502901), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860009502901 UDI-DI Date23 Feb 2023ListedStatusListed 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  • Withdrawn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
Wound CareKit
Generic name
Wound dressing kit, non-medicated
Model / Ref / Catalog
MDXWC02, MDXWC021
Primary DI / UDI-DI
00860009502901
FDA product code
MCY
GMDN term
Wound dressing kit, non-medicated
Device class
Class II
Regulation number
880.5075
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MCY (Wound Dressing Kit).

Other devices from Mirodx, LLC

See all devices from Mirodx, LLC →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)