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710 Allure 711N

by Sigvaris, Inc. GUDID 30 variants

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00745129264444 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  • Withdrawn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

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
710 Allure
Generic Name
Compression/pressure sock/stocking, single-use
Model / Ref / Catalog
711N, 711NSSW13
Primary DI / UDI-DI
00745129264444
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.

See all devices from Sigvaris, Inc. →

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