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Escalon ISPAN

by Airgas Therapeutics

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 Number00819601025837 UDI-DI Date21 Nov 2025ListedStatusListed 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  • Withdrawn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
Escalon
Generic Name
Intraocular gas cylinder regulator
Model / Ref / Catalog
ISPAN, SMPQES180@V2
Primary DI / UDI-DI
00819601025837
FDA Product Code
CAN
GMDN Term
Intraocular gas cylinder regulator
Device Class
Class I
Regulation Number
868.2700
GUDID distribution status
In Commercial Distribution

Other devices from Airgas Therapeutics

See all devices from Airgas Therapeutics →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No