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Centurion M12013KNL

by Centurion Medical Products

Centurion M12013KNL is a Class II device made by Centurion Medical Products, listed in FDA GUDID since 14 Sep 2016 (UDI-DI 10653160247593), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10653160247593 UDI-DI Date14 Sep 2016ListedStatusListed 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  • Withdrawn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
Centurion
Generic name
Central venous catheterization kit, short-term
Model / reference
M12013KNL
Primary DI / UDI-DI
10653160247593
FDA product code
OES
GMDN term
Central venous catheterization kit, short-term
Device class
Class II
Regulation number
870.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Central venous catheterization kit, short-term

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)