Centurion SP2230

by Centurion Medical Products

Centurion SP2230 is a Class I device made by Centurion Medical Products, listed in FDA GUDID since 2 Jan 2022 (UDI-DI 10653160289777), registry data as of 23 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10653160289777 UDI-DI	Date2 Jan 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10653160289777

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Centurion
Generic name: Surgical patient preparation kit
Model / Ref / Catalog: SP2230

Primary DI / UDI-DI: 10653160289777
FDA product code: OJU
GMDN term: Surgical patient preparation kit

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)