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Centurion CVI4380

by Centurion Medical Products

Centurion CVI4380 is a Class II device made by Centurion Medical Products, listed in FDA GUDID since 14 Aug 2017 (UDI-DI 10653160310020), 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 Number10653160310020 UDI-DI Date14 Aug 2017ListedStatusListed 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  • Withdrawn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
Centurion
Generic name
Peripheral intravenous catheterization support kit
Model / reference
CVI4380
Primary DI / UDI-DI
10653160310020
FDA product code
LRS
GMDN term
Peripheral intravenous catheterization support kit
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LRS (I.V. start kit).

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)