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Deltaven 3836372

by Delta Med SpA

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08032248383630 UDI-DI Date19 Jan 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Deltaven
Generic name
Peripheral vascular catheter
Model / reference
3836372
Primary DI / UDI-DI
08032248383630
FDA product code
FOZ
GMDN term
Peripheral vascular catheter
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 1.00 Millimeter
Length — 32 Millimeter

Related devices

Category: Peripheral vascular catheter

Other devices from Delta Med SpA

See all devices from Delta Med SpA →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (9)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No