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Corepoint NSBF231WSWCR/0

by Horizon Scientific, Inc.

Corepoint NSBF231WSWCR/0 is a Class II device made by Horizon Scientific, Inc., listed in FDA GUDID since 10 Dec 2021 (UDI-DI 00810083952826), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810083952826 UDI-DI Date10 Dec 2021ListedStatusListed 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  • Withdrawn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
Corepoint
Generic name
Blood refrigerator/freezer
Model / reference
NSBF231WSWCR/0
Primary DI / UDI-DI
00810083952826
FDA product code
KSE
GMDN term
Blood refrigerator/freezer
Device class
Class II
Regulation number
864.9700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood refrigerator/freezer

Similar devices

Other devices filed under FDA product code KSE (Refrigerator, Freezer, Blood Storage).

Other devices from Horizon Scientific, Inc.

See all devices from Horizon Scientific, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)