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Coronet 51-900-8.25

by Network Medical Products, Ltd.

Coronet 51-900-8.25 is a Class I device made by Network Medical Products, Ltd., listed in FDA GUDID since 7 Aug 2019 (UDI-DI 05060165011643), 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 Number05060165011643 UDI-DI Date7 Aug 2019ListedStatusListed 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  • Withdrawn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
Corneal trephine, single-use
Model / reference
51-900-8.25
Primary DI / UDI-DI
05060165011643
FDA product code
HRH
GMDN term
Corneal trephine, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Corneal trephine, single-use

Similar devices in this category

Other devices filed under Corneal trephine, single-use.

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
  • Expiration date
Other properties (10, all answered No)