Skip to content

Bracket Arterial Filter

by LivaNova USA, Inc.

Bracket Arterial Filter is a medical device service rail clamp (FDA Class I; FDA product code KRI, Accessory Equipment, Cardiopulmonary Bypass) made by LivaNova USA, Inc., listed in FDA GUDID since 13 May 2016 (UDI-DI 00803622131752), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00803622131752 UDI-DI Date13 May 2016ListedStatusListed 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  • Withdrawn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
Bracket
Generic name
Medical device service rail clamp
Model / reference
Arterial Filter
Primary DI / UDI-DI
00803622131752
FDA product code
KRI
GMDN term
Medical device service rail clamp
Device class
Class I
Regulation number
870.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical device service rail clamp

Similar devices in this category

Other devices filed under Medical device service rail clamp.

Other devices from LivaNova USA, Inc.

  • Perfusion Pack

    Class II

  • Perfusion Pack

    Class II

  • Perfusion Pack

    Class II

  • Perfusion Pack

    Class II

See all devices from LivaNova USA, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)