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710 Allure 711P

by Sigvaris, Inc. 30 variants

Listed FDA GUDID listing, not in commercial distribution

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 Number00745129264468 UDI-DIDate12 Feb 2019ListedStatusListed GUDID: not 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  • Withdrawn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
710 Allure
Generic Name
Compression/pressure sock/stocking, single-use
Model / Ref / Catalog
711P, 711PLSW13
Primary DI / UDI-DI
00745129264468
FDA Product Code
FQL
GMDN Term
Compression/pressure sock/stocking, single-use
Device Class
Class I
Regulation Number
880.5780
GUDID distribution status
Not in Commercial Distribution

Other devices from Sigvaris, Inc.

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Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No