MedtechSourcebook

CAREFUSION 2200, INC.

Contract manufacturer · Mannford, OK

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration
1625685 (openFDA record; or search FDA's registration database)
FEI number
1625685
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
CAREFUSION (FDA owner/operator no. 10030506)
Registered address
400 East Foster Rd, Mannford, OK 74044
Contract listings
12 device listings, 11 product codes, first listed Oct 12, 2009
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
DWMApparatus, Suction, Patient CareClass IICardiovascularContract manufacturingNov 22, 2016
DYBIntroducer, CatheterClass IICardiovascularContract manufacturingFeb 7, 2018
FCGBiopsy NeedleClass IIGastroenterology and urologyContract manufacturingOct 12, 2009
FMINeedle, Hypodermic, Single LumenClass IIGeneral hospitalContract manufacturingOct 12, 2009
FSHTray, Surgical, NeedleClass IGeneral and plastic surgeryContract manufacturingOct 12, 2009
KNWInstrument, BiopsyClass IIGastroenterology and urologyContract manufacturingSep 12, 2017
KPMShunt, PeritonealClass IIGastroenterology and urologyContract manufacturingOct 12, 2009
LWEBone Marrow Collection/Transfusion KitClass IIGeneral hospitalContract manufacturingOct 12, 2009
MDMInstrument, Manual, Surgical, General UseClass IGeneral and plastic surgeryContract manufacturingOct 12, 2009
PNGPeritoneal, Drainage Catheter For Refractory Ascites, Long-Term IndwellingClass IIGastroenterology and urologyContract manufacturingJan 9, 2025
PXIThoracentesis TrayClass IIGeneral hospitalContract manufacturingApr 15, 2019