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Stoploss® Jones Tube 3, 5 X 11 Mm S1.7311

by Fci S a S Fci 20 22

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 Number13700773729675 UDI-DI Date20 Apr 2026ListedStatusListed 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  • Withdrawn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
Stoploss® Jones Tube 3,5 X 11 Mm
Generic Name
Lacrimal tube
Model / Reference
S1.7311
Primary DI / UDI-DI
13700773729675
FDA Product Code
OKS
GMDN Term
Lacrimal tube
Device Class
U
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Fci S a S Fci 20 22

See all devices from Fci S a S Fci 20 22 →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No