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SURGI-PVA™- Eye Wick EYW 200

by Aegis Lifesciences Private Limited

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 Number08906038453141 UDI-DI Date20 Aug 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  • Withdrawn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
SURGI-PVA™- Eye Wick
Generic Name
Ophthalmic sponge
Model / Ref / Catalog
EYW 200
Primary DI / UDI-DI
08906038453141
FDA Product Code
HOZ
GMDN Term
Ophthalmic sponge
Device Class
Class II
Regulation Number
886.4790
GUDID distribution status
In Commercial Distribution
Size
Length — 200 Millimeter
Width — 3 Millimeter
Height — 2 Millimeter

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Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

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