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Core-Spun® 18442

by Thuasne, LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00721734184421 UDI-DI Date5 Jan 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Core-Spun®
Generic name
Compression/pressure sock/stocking, single-use
Model / reference
18442
Description
20-30 mmHg CORESPUN SOCKS SMALL NAVY
Primary DI / UDI-DI
00721734184421
FDA product code
FQL, DWL
GMDN term
Compression/pressure sock/stocking, single-use
Device class
Class I
Regulation number
880.5780
GUDID distribution status
In Commercial Distribution

Related devices

Category: Compression/pressure sock/stocking, single-use

Other devices from Thuasne, LLC

See all devices from Thuasne, LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No