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Cardinal Health PVSVVP532

by Cardinal Health 200, LLC GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10195594676216 UDI-DIDate17 May 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Cardinal Health
Generic Name
Cardiothoracic surgical procedure kit, medicated, single-use
Model / Ref / Catalog
PVSVVP532
Primary DI / UDI-DI
10195594676216
FDA Product Code
OEZ
GMDN Term
Cardiothoracic surgical procedure kit, medicated, single-use
Device Class
Class II
Regulation Number
870.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiothoracic surgical procedure kit, medicated, single-use

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (5)

  • Implantable: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No