Bear 6.40.03

by Bear-Ent, LLC

Bear 6.40.03 is a Class I device made by Bear-Ent, LLC, listed in FDA GUDID since 1 Aug 2022 (UDI-DI G043640030), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberG043640030 UDI-DI	Date1 Aug 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Bear
Generic name: Ear canal irrigation syringe
Model / Ref / Catalog: 6.40.03

Primary DI / UDI-DI: G043640030
FDA product code: KCP
GMDN term: Ear canal irrigation syringe

Device class: Class I
Regulation number: 874.5220
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)