FDA UDI In Commercial Distribution 🇺🇸 United States

LifeSPARC

DI: 00814112020807 · Model: 5820-3631 · CARDIACASSIST, INC.
Product Codes
5
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LifeSPARC
Primary DI
00814112020807
Version / Model
5820-3631
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-18
Public Version
3
Public Version Date
2023-03-13
Public Version Status
Update
Public Device Record Key
655abc15-a08c-4ef1-ad7d-065dcd47081f

Device Description

LifeSPARC Blood Pump Kit with 31 Fr ProtekDuo Veno-Venous Rapid Depolyment Cannula

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DRE Dilator, Vessel, For Percutaneous Catheterization
KRI Accessory Equipment, Cardiopulmonary Bypass
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
QNR Blood Pump For Ecmo, Long-Term (> 6 Hours) Use

GMDN Terms

Code Name
38128 Vascular dilator, single-use
36373 Cardiopulmonary bypass system mounting unit
31718 Cardiopulmonary bypass system centrifugal pump
58726 Mobile extracorporeal gas exchange system catheter kit

Identifiers

Type ID
Primary 00814112020807

Customer Contacts

Phone
18003737421
Phone
+14129637770