FDA UDI In Commercial Distribution 🇺🇸 United States

DLP®

DI: 20643169454464 · Model: 94913L · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
DLP®
Primary DI
20643169454464
Version / Model
94913L
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-05-22
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
73f8c4e4-5a0e-4177-8e09-ec0e102458d0

Device Description

CANNULA 94913L RCSP SIL MAN 13F 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
36109 Coronary sinus cannula

Identifiers

Type ID
Primary 20643169454464
Unit of Use 00643169454460

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K953945 000

Device Sizes

Type Value Unit Text
Catheter Gauge 13.0 French