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Brite Tip 401423M

by Cordis US Corp.

Brite Tip 401423M is a Class II device made by Cordis US Corp., listed in FDA GUDID since 1 Aug 2016 (UDI-DI 10705032000161), 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 Number10705032000161 UDI-DI Date1 Aug 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  • Withdrawn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
Brite Tip
Generic name
Haemostasis valve
Model / Ref / Catalog
401423M
Primary DI / UDI-DI
10705032000161
FDA product code
DYB
GMDN term
Haemostasis valve
Device class
Class II
Regulation number
870.1340
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemostasis valve

Similar devices in this category

Other devices filed under Haemostasis valve.

Other devices from Cordis US Corp.

See all devices from Cordis US Corp. →

Properties

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