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Ruby Intravascular Catheter VNC20130FG

by Venocare, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850073657003 UDI-DI Date8 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ruby Intravascular Catheter
Generic Name
Peripheral intravenous cannula
Model / Reference
VNC20130FG
Primary DI / UDI-DI
00850073657003
510(k) Number
FDA Product Code
FOZ
GMDN Term
Peripheral intravenous cannula
Device Class
Class II
Regulation Number
880.5200
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K244047)

Other devices from Venocare, Inc.

See all devices from Venocare, Inc. →

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