Aerosizer® 00884450031117

by Merit Medical Systems, Inc.

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	Number00884450031117 UDI-DI	Date4 Oct 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Aerosizer®
Generic Name: Endoscopic measuring device, pulmonary stricture
Model / Ref / Catalog: 00884450031117, 90129-501/C

Primary DI / UDI-DI: 00884450031117
FDA Product Code: FDY
GMDN Term: Endoscopic measuring device, pulmonary stricture

Device Class: Class I
Regulation Number: 876.1500
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Conditional

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Class IIb
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See all devices from Merit Medical Systems, Inc. →

Properties

Single Use
Premarket Exempt
Lot / Batch Number
Expiration 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
Manufacturing Date: No