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Bear 1.11.54

by Bear-Ent, LLC

Bear 1.11.54 is a Class I device made by Bear-Ent, LLC, listed in FDA GUDID since 8 Jul 2026 (UDI-DI G043111540), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG043111540 UDI-DI Date8 Jul 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Bear
Generic name
Surgical/emergency suction cannula, non-illuminating, reusable
Model / Ref / Catalog
1.11.54
Primary DI / UDI-DI
G043111540
FDA product code
JZF
GMDN term
Surgical/emergency suction cannula, non-illuminating, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Bear-Ent, LLC

See all devices from Bear-Ent, LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)