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Vmax 63811

by Carefusion GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10846446027716 UDI-DIDate16 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Vmax
Generic Name
Pulmonary function analysis system, paediatric
Model / Ref / Catalog
63811
Primary DI / UDI-DI
10846446027716
FDA Product Code
BTY
GMDN Term
Pulmonary function analysis system, paediatric
Device Class
Class II
Regulation Number
868.1890
GUDID distribution status
Not in Commercial Distribution

Other devices from Carefusion

See all devices from Carefusion →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single 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
  • Expiration Date: No