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Sharn Inc S2020-M

by Sharn Anesthesia

Sharn Inc S2020-M is a Class I device made by Sharn Anesthesia, listed in FDA GUDID since 16 Nov 2018 (UDI-DI 00817518022147), 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 Number00817518022147 UDI-DI Date16 Nov 2018ListedStatusListed 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  • Withdrawn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

Trade name
Sharn Inc
Generic name
Eye patch, single-use
Model / Ref / Catalog
S2020-M
Primary DI / UDI-DI
00817518022147
FDA product code
HOY
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye patch

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Other devices filed under Eye patch.

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)