FDA UDI In Commercial Distribution 🇺🇸 United States

TandemHeart

DI: 00814112020371 · Model: 5710-6215 · CARDIACASSIST, INC.
Product Codes
2
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TandemHeart
Primary DI
00814112020371
Version / Model
5710-6215
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-25
Public Version
5
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
9a750a4e-109f-49eb-b335-5fccf7ddaa32

Device Description

TandemHeart blood pump kit with 62cm venous and 15Fr arterial cannulae

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
Labeling does not contain MRI Safety Information
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
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

GMDN Terms

Code Name
47733 Cardiopulmonary bypass cannula, femoral
31718 Cardiopulmonary bypass system centrifugal pump
46849 Circulatory assist transseptal cannula

Identifiers

Type ID
Primary 00814112020371

Customer Contacts

Phone
18003737421
Phone
+14129637770

Premarket Submissions

Submission Number Supplement Number
K052570 000
K110493 000
K133293 000