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BR Surgical, LLC BR46-39002

by Br Surgical LLC

BR Surgical, LLC BR46-39002 is a Class I device made by Br Surgical LLC, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 00840183531058), 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 Number00840183531058 UDI-DI Date17 Jul 2026ListedStatusListed 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  • Withdrawn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
Nasal knife
Model / Ref / Catalog
BR46-39002
Primary DI / UDI-DI
00840183531058
FDA product code
KTG
GMDN term
Nasal knife
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Other devices from Br Surgical LLC

See all devices from Br Surgical LLC →

Properties

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