FDA UDI Not in Commercial Distribution 🇺🇸 United States

DLP®

DI: 20643169086801 · Model: 82024 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
DLP®
Primary DI
20643169086801
Version / Model
82024
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-06-17
Public Version
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
1b3a575c-a2ff-4e83-83b3-bb4b4b220484
Distribution End Date
2017-08-25

Device Description

CANNULA 82024 ART CUR TIP 24FR 20PK 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, arterial

Identifiers

Type ID
Primary 20643169086801
Unit of Use 00643169086807

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K840002 000

Device Sizes

Type Value Unit Text
Catheter Gauge 24.0 French