710 Allure 712P

by Sigvaris, Inc. 30 variants

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00745129217358 UDI-DI	Date9 Nov 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: 712P, 712PSSW91

Primary DI / UDI-DI: 00745129217358
FDA Product Code: FQL
GMDN Term: Compression/pressure sock/stocking, single-use

Device Class: Class I
Regulation Number: 880.5780
GUDID distribution status: In Commercial Distribution

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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