FDA UDI Not in Commercial Distribution 🇺🇸 United States

DLP®

DI: 20613994879121 · Model: 69531 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
DLP®
Primary DI
20613994879121
Version / Model
69531
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-06-17
Public Version
5
Public Version Date
2022-09-22
Public Version Status
Update
Public Device Record Key
788da736-c23c-4e6c-91c2-8ada930cbab7
Distribution End Date
2019-10-21

Device Description

CANNULA 69531 VEN RT METAL 31FR 5HL 10PK

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
34905 Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, venous

Identifiers

Type ID
Primary 20613994879121
Unit of Use 00613994879127

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 31.0 French