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Coronet 53-956

by Network Medical Products, Ltd.

Coronet 53-956 is a Class I device made by Network Medical Products, Ltd., listed in FDA GUDID since 27 Aug 2020 (UDI-DI 05056100704374), 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 Number05056100704374 UDI-DI Date27 Aug 2020ListedStatusListed 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  • Withdrawn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
Coronet
Generic name
Donor cornea delivery set
Model / reference
53-956
Primary DI / UDI-DI
05056100704374
FDA product code
HNR
GMDN term
Donor cornea delivery set
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Donor cornea delivery set

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)