FDA UDI In Commercial Distribution 🇺🇸 United States

ThruPort Systems Arterial Cannula Kit

DI: 00690103182606 · Model: AC19 · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ThruPort Systems Arterial Cannula Kit
Primary DI
00690103182606
Version / Model
AC19
Catalog Number
AC19
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
1d36808a-1665-48ef-a2d8-b062f3e65c43

Device Description

Arterial Cannula 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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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

GMDN Terms

Code Name
34893 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, arterial

Identifiers

Type ID
Primary 00690103182606

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K971291 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 19 Fr. (6.3 mm) X 3.7" (9.4 cm)

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store sterile packaged device in a cool dry place.