Lieberman Adjustable/Aspirating Speculum Ae-1040AN

by Katena Products, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841668126752 UDI-DI	Date7 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Lieberman Adjustable/Aspirating Speculum
Generic Name: Eyelid speculum, reusable
Model / Ref / Catalog: AE-1040AN

Primary DI / UDI-DI: 00841668126752
FDA Product Code: HNC
GMDN Term: Eyelid speculum, reusable

Device Class: Class I
Regulation Number: 886.4350
GUDID distribution status: In Commercial Distribution

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Properties

Prescription Use
Premarket Exempt

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Lot / Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No