FDA UDI Not in Commercial Distribution 🇺🇸 United States

EOPA CAP™

DI: 20643169486212 · Model: 77818 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
EOPA CAP™
Primary DI
20643169486212
Version / Model
77818
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
c17a6d44-9acc-46c1-9ac1-82f24998823e
Distribution End Date
2017-08-25

Device Description

CANNULA 77818 EOPA CAP 18FR 10PK 10L

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
No
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 20643169486212
Unit of Use 00643169486218

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K031518 000

Device Sizes

Type Value Unit Text
Catheter Gauge 18.0 French