FDA UDI In Commercial Distribution 🇺🇸 United States

EOPA™

DI: 20763000135649 · Model: 77424 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
EOPA™
Primary DI
20763000135649
Version / Model
77424
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-03-03
Public Version
5
Public Version Date
2023-08-04
Public Version Status
Update
Public Device Record Key
1f7dbae7-2ad4-459b-a971-fffb653f9533

Device Description

CANNULA 77424 EOPA BLUNT 24FR 10PK 11L

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 20763000135649
Unit of Use 00763000135645

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K031037 000

Device Sizes

Type Value Unit Text
Catheter Gauge 24.0 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius