FDA UDI In Commercial Distribution 🇺🇸 United States

ProtekDuo

DI: 00814112020555 · Model: 5730-3631 · CARDIACASSIST, INC.
Product Codes
5
GMDN Terms
6
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProtekDuo
Primary DI
00814112020555
Version / Model
5730-3631
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-08
Public Version
3
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
6a6f2249-2645-4453-8037-7e8a0a6bd81d

Device Description

TandemHeart Blood Pump Kit with 31 Fr Mini V-V cannula, TandemLung Oxygentor

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
DRE Dilator, Vessel, For Percutaneous Catheterization

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
38128 Vascular dilator, single-use
58726 Mobile extracorporeal gas exchange system catheter kit

Identifiers

Type ID
Primary 00814112020555

Customer Contacts

Phone
+14129637770
Phone
18003737421