NA Featherweight Leg Section

by Steris Corporation 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	Number00724995221584 UDI-DI	Date24 Jun 2026Listed	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Withdrawn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

Generic Name: Leg procedure positioner
Model / Ref / Catalog: Featherweight Leg Section, BF020

Primary DI / UDI-DI: 00724995221584
FDA Product Code: FQO
GMDN Term: Leg procedure positioner

Device Class: Class I
Regulation Number: 878.4960
GUDID distribution status: In Commercial Distribution

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Properties

Over-the-Counter
Premarket Exempt
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Lot / Batch Number: No
Serial Number: No
Expiration Date: No