Centurion EC1000ST

by Centurion Medical Products

Centurion EC1000ST is a Class I device made by Centurion Medical Products, listed in FDA GUDID since 1 Jan 2022 (UDI-DI 00653160093247), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00653160093247 UDI-DI	Date1 Jan 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00653160093247

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Centurion
Generic name: General surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog: EC1000ST

Primary DI / UDI-DI: 00653160093247
FDA product code: MDM
GMDN term: General surgical procedure kit, non-medicated, single-use

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
Premarket exempt
Lot / batch number
Expiration date

Other properties (9, all answered No)