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Bear 6.11.32

by Bear-Ent, LLC

Bear 6.11.32 is a Class I device made by Bear-Ent, LLC, listed in FDA GUDID since 3 Apr 2022 (UDI-DI G043611320), 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 NumberG043611320 UDI-DI Date3 Apr 2022ListedStatusListed 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  • Withdrawn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
Endaural surgical curette, reusable
Model / Ref / Catalog
6.11.32
Primary DI / UDI-DI
G043611320
FDA product code
JYG
GMDN term
Endaural surgical curette, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endaural surgical curette, reusable

Similar devices in this category

Other devices filed under Endaural surgical curette, reusable.

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Properties

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