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BR Surgical, LLC BR46-29507

by Br Surgical LLC

BR Surgical, LLC BR46-29507 is a Class I device made by Br Surgical LLC, listed in FDA GUDID since 13 Nov 2023 (UDI-DI 00840183502249), 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 Number00840183502249 UDI-DI Date13 Nov 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
BR Surgical, LLC
Generic name
Surgical/emergency suction cannula, non-illuminating, reusable
Model / Ref / Catalog
BR46-29507
Primary DI / UDI-DI
00840183502249
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

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Similar devices in this category

Other devices filed under Surgical/emergency suction cannula, non-illuminating, reusable.

Other devices from Br Surgical LLC

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)