710 Allure 712P

by Sigvaris, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00745129217327 UDI-DI	Date9 Nov 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: 712P, 712PSLW91

Primary DI / UDI-DI: 00745129217327
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