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600-30

by Eagle Labs, LLC

600-30 is a Class II device made by Eagle Labs, LLC, listed in FDA GUDID since 28 Oct 2016 (UDI-DI 00810090013916), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810090013916 UDI-DI Date28 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Ophthalmic sponge
Model / reference
600-30
Primary DI / UDI-DI
00810090013916
FDA product code
HOZ
GMDN term
Ophthalmic sponge
Device class
Class II
Regulation number
886.4790
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization
Size
Lumen/Inner Diameter — 9.5 Millimeter

Related devices

Category: Ophthalmic sponge

Similar devices in this category

Other devices filed under Ophthalmic sponge.

Other devices from Eagle Labs, LLC

See all devices from Eagle Labs, LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)