AccessGUDID - DEVICE: FloPump (00814321020124)

GUDID

Device Identifier (DI) Information

Brand Name: FloPump
Version or Model: 1/4" FloPump (Non-Sterile)
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 6300N
Company Name: Movair, Inc.

Primary DI Number: 00814321020124
Issuing Agency: GS1
Commercial Distribution End Date: December 13, 2021
Device Count: 1
Labeler D-U-N-S® Number*: 788403103 *Terms of Use

Device Description: The IBC FloPump is a single-use, disposable centrifugal blood pump intended for use only with the Medtronic Bio Medicus Bio-Console to pump blood through the extracorporeal bypass circuit during open heart surgery.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
31718	Cardiopulmonary bypass system centrifugal pump	A device intended to be connected to a drive unit (not included) to circulate blood through the extracorporeal circuit of a non-roller type cardiopulmonary bypass system, via a centrifugal force mechanism, for gas exchange and reinfusion; it may in addition be used in extracorporeal support systems for ventricular support/circulatory assistance. It includes flow channels and a rotor driven by the system’s drive unit. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KFM	Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K983272	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Ethylene Oxide

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 0cf7ec3a-b115-4c61-a62b-1cc96cbe3e15
Public Version Date: February 24, 2025
Public Version Number: 6
DI Record Publish Date: November 09, 2015