Skip to content

Centurion I550BF85NL

by Centurion Medical Products

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10653160248477 UDI-DI Date13 Sep 2016ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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
I550BF85NL
Primary DI / UDI-DI
10653160248477
FDA Product Code
OFD
GMDN Term
Central venous catheterization kit, short-term
Device Class
Class II
Regulation Number
870.1340
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

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No