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810-60

by Eagle Labs, LLC

810-60 is a Class II device made by Eagle Labs, LLC, listed in FDA GUDID since 28 Oct 2016 (UDI-DI 00810090011448), 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 Number00810090011448 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  • Withdrawn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 surgical drape
Model / reference
810-60
Primary DI / UDI-DI
00810090011448
FDA product code
HMT
GMDN term
Ophthalmic surgical drape
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Area/Surface Area — 2400 Square inch

Related devices

Category: Ophthalmic surgical drape

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)