FDA UDI In Commercial Distribution 🇺🇸 United States

DLP™

DI: 20199150023220 · Model: 77114 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
DLP™
Primary DI
20199150023220
Version / Model
77114
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2025-11-02
Public Version
1
Public Version Date
2025-11-10
Public Version Status
New
Public Device Record Key
5259edf2-a4e6-484a-a0c1-47e2e877b131

Device Description

CANNULA 77114 ART ONE PIECE 14FR 5PK 17

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
Unit of Use 00199150023226
Primary 20199150023220

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K024069 000

Device Sizes

Type Value Unit Text
Catheter Gauge 14.0 French