FDA UDI In Commercial Distribution 🇺🇸 United States

TandemLife

DI: 00814112020494 · Model: 5180-0000 · CARDIACASSIST, INC.
Product Codes
4
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TandemLife
Primary DI
00814112020494
Version / Model
5180-0000
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-07
Public Version
5
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
456708a8-1f31-47f9-afdb-e2a924ea0159

Device Description

TandemLife Priming Tray Kit: TandemHeart Blood Pump with TandemLung Oxygenator

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
No
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
KRI Accessory Equipment, Cardiopulmonary Bypass
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
DTZ Oxygenator, Cardiopulmonary Bypass

GMDN Terms

Code Name
46846 Mechanical infusion pump administration set
36373 Cardiopulmonary bypass system mounting unit
31718 Cardiopulmonary bypass system centrifugal pump
17643 Extracorporeal membrane oxygenator

Identifiers

Type ID
Primary 00814112020494

Customer Contacts

Phone
18003737421
Phone
+14129637770