FDA UDI In Commercial Distribution 🇺🇸 United States

Percutaneous Insertion Kit-Arterial

DI: 00690103033250 · Model: PIKA · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Percutaneous Insertion Kit-Arterial
Primary DI
00690103033250
Version / Model
PIKA
Catalog Number
PIKA
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
afedba21-2562-45a7-94c0-92c4a9bae93c

Device Description

Percutaneous Insertion Kit-Arterial

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
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Primary 00690103033250
Package 50690103033255

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K140208 000