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VueBlu 5000311

by Cosmo 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 Number05391530190527 UDI-DI Date21 Jul 2023ListedStatusListed 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  • Withdrawn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
VueBlu
Generic Name
Operative procedure tissue/fluid stain
Model / Reference
5000311
Primary DI / UDI-DI
05391530190527
FDA Product Code
NBG
GMDN Term
Operative procedure tissue/fluid stain
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 10 Milliliter

Related devices

Category: Operative procedure tissue/fluid stain

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

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