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Caphosol® Artifical Saliva 64 x 15 mL sachets aqueous solution

by Eusa Pharma (Uk) Limited

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060146293129 UDI-DI Date26 Jun 2024ListedStatusListed GUDID: not 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  • Withdrawn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
Caphosol® Artifical Saliva
Generic Name
Artificial saliva
Model / Reference
64 x 15 mL sachets aqueous solution
Primary DI / UDI-DI
05060146293129
FDA Product Code
LFD
GMDN Term
Artificial saliva
Device Class
U
GUDID distribution status
Not in Commercial Distribution

Other devices from Eusa Pharma (Uk) Limited

Properties

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

Other properties (10)

  • Sterile: 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
  • Manufacturing Date: No