FDA UDI In Commercial Distribution 🇺🇸 United States

TandemLung

DI: 00814112020241 · Model: 5160-0000 · CARDIACASSIST, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TandemLung
Primary DI
00814112020241
Version / Model
5160-0000
Company Name
CARDIACASSIST, INC.
Labeler DUNS
948683941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-06
Public Version
5
Public Version Date
2020-01-22
Public Version Status
Update
Public Device Record Key
2d3b6ec3-2a0f-4e9c-8fc6-bb24eb78f51b

Device Description

TandemLung Oxygenator Kit with accessories

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
DTZ Oxygenator, Cardiopulmonary Bypass

GMDN Terms

Code Name
17643 Extracorporeal membrane oxygenator

Identifiers

Type ID
Primary 00814112020241

Customer Contacts

Phone
+18003737421
Phone
+14129637770

Premarket Submissions

Submission Number Supplement Number
K153295 000