FDA UDI Not in Commercial Distribution 🇺🇸 United States

FloPump

DI: 00814321020131 · Model: 6400S · Movair, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FloPump
Primary DI
00814321020131
Version / Model
6400S
Catalog Number
6400S
Company Name
Movair, Inc.
Labeler DUNS
788403103
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-18
Public Version
6
Public Version Date
2025-02-24
Public Version Status
Update
Public Device Record Key
39aa32bb-0c45-4999-82bd-f46915678f6e
Distribution End Date
2021-12-13

Device Description

The FloPump 32mL Centrifugal Pump is a device that uses a method other than revolving rollers to pump the blood through an extracorporeal circuit for periods lasting less than 6 hours for the purpose of providing either: i) Full or partial cardiopulmonary bypass (i.e., circuit includes an oxygenator) during open surgical procedures on the heart or great vessels; or ii) Temporary circulatory bypass for diversion offlow around a planned disruption of the circulatory pathway necessary for open surgical procedures on the aorta or vena cava.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
31718 Cardiopulmonary bypass system centrifugal pump

Identifiers

Type ID
Primary 00814321020131

Premarket Submissions

Submission Number Supplement Number
K170029 000