FDA UDI In Commercial Distribution 🇺🇸 United States

TandemLife

DI: 00814112020500 · Model: 5180-0001 · CARDIACASSIST, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TandemLife
Primary DI
00814112020500
Version / Model
5180-0001
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
3
Public Version Date
2018-10-03
Public Version Status
Update
Public Device Record Key
133fc0b2-b09a-4613-ae9f-6f1a0c7dc77a

Device Description

TandemLife Priming Tray Accessory Kit

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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

GMDN Terms

Code Name
46846 Mechanical infusion pump administration set
36373 Cardiopulmonary bypass system mounting unit

Identifiers

Type ID
Primary 00814112020500

Customer Contacts

Phone
18003737421
Phone
14129637770