FDA UDI In Commercial Distribution 🇺🇸 United States

EOPA 3D®

DI: 20643169486243 · Model: 78220 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
EOPA 3D®
Primary DI
20643169486243
Version / Model
78220
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-06-13
Public Version
5
Public Version Date
2024-06-19
Public Version Status
Update
Public Device Record Key
9c1f88d3-6ca7-45a6-b1a8-403fe2f1ee94

Device Description

CANNULA 78220 EOPA 3D 20FR VNTED 10P 17L

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, return

Identifiers

Type ID
Primary 20643169486243
Unit of Use 00643169486249

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150422 000

Device Sizes

Type Value Unit Text
Catheter Gauge 20.0 French