HarmonyAIR A-Series Suspension System

by Steris Corporation

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	Number00724995216016 UDI-DI	Date5 Nov 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: HarmonyAIR
Generic Name: Medical monitor/light mount
Model / Ref / Catalog: A-Series Suspension System, LAH0055A

Primary DI / UDI-DI: 00724995216016
FDA Product Code: FQO
GMDN Term: Medical monitor/light mount

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

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Properties

Over-the-Counter
Premarket Exempt
Serial Number
Manufacturing Date

Other properties (10)

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
Expiration Date: No