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Velox Pro VP14200-C0

by Medax Unipersonale Srl

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number08055002900324 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Velox Pro
Generic Name
Needle guide, single-use
Model / Reference
VP14200-C0
Primary DI / UDI-DI
08055002900324
510(k) Number
FDA Product Code
KNW
GMDN Term
Needle guide, single-use
Device Class
Class II
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Needle guide, single-use

Cleared under the same submission (K092338)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No